Prof. Dr. HALİL SAĞLAM

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.31, sa.10, ss.1091-1098, 2018 (SCI-Expanded)

Chromhidrosis due to exogenous oxidizing heavy metals: Clinical and laboratory findings.

ERDÖL Ş., Karakaya S., SAĞLAM H., Tarim Ö. F.

Pediatric dermatology , cilt.35, sa.4, ss.448-452, 2018 (SCI-Expanded)

Outcomes of mitochondrial derived diseases: a single-center experience

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.31, sa.4, ss.399-405, 2018 (SCI-Expanded)

Clinical and Genetic Findings of Turkish Hypophosphatasia Cases

SAĞLAM H., ERDÖL Ş., Dorum S.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, sa.3, ss.229-236, 2017 (SCI-Expanded)

Delayed Puberty and Gonadal Failure in Patients with HAX1 Mutation

ÇEKİÇ Ş., SAĞLAM H., Gorukmez O., Yakut T., Tarim Ö. F., Kilic S. Ş.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.37, sa.6, ss.524-528, 2017 (SCI-Expanded)

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

Baric I., ERDÖL Ş., SAĞLAM H., Lovric M., Beluzic R., Vugrek O., et al.

JIMD REPORTS, VOL 31 , cilt.31, ss.101-106, 2017 (SCI-Expanded)

CLINICAL AND LABORATORY CHARACTERISTICS OF HYPERPROLACTINEMIC CHILDREN AND ADOLESCENTS: NATIONAL SURVEY

EREN E., Ergur A. T., İŞGÜVEN Ş. P., Bitkin E. C., BERBEROĞLU M., ŞIKLAR Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.313-314, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ

Nicholas A. K., Serra E. G., CANGÜL H., Alyaarubi S., Ullah I., Schoenmakers E., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.101, sa.12, ss.4521-4531, 2016 (SCI-Expanded)

An Unusual Case of LCHAD Deficiency Presenting With a Clinical Picture of Hemophagocytic Lymphohistiocytosis: Secondary HLH or Coincidence?

ERDÖL Ş., Ture M., Baytan B., Yakut T., SAĞLAM H.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.38, sa.8, ss.661-662, 2016 (SCI-Expanded)

Evaluation of therapeutics management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey: A nationwide cross-sectional study

Hatun S., Demirbilek H., DARCAN Ş., Yuksel A., Binay C., Simsek D. G., et al.

DIABETES RESEARCH AND CLINICAL PRACTICE , cilt.119, ss.32-40, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases

Demirkaya M., Sevinir B. B., Sağlam H.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.8, sa.3, ss.330-333, 2016 (SCI-Expanded)

Massive ascites in a canakinumab resistant case with MVA leading to bone marrow transplantation.

ERDÖL Ş., ÇEKİÇ Ş., Kilic S. C., SAĞLAM H., Kilic S. Ş.

Rheumatology international , cilt.36, sa.7, ss.1011-3, 2016 (SCI-Expanded)

Celiac Disease Presenting with Biotinidase Deficiency and Paraplegia

ERDÖL Ş., SAĞLAM H., Basarir T. O., OKAN M. S.

INDIAN JOURNAL OF PEDIATRICS , cilt.83, sa.6, ss.596-597, 2016 (SCI-Expanded)

The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study

Atay Z., Yesilkaya E., Erdeve S. S., DEMİRCİOĞLU S., AKIN L., EREN E., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.101, sa.5, ss.1980-1988, 2016 (SCI-Expanded)

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome.

Sari E., BEREKET A., Yesilkaya E., Bas F., Bundak R., Aydin B. K., et al.

American journal of medical genetics. Part A , sa.4, ss.942-8, 2016 (SCI-Expanded)

Retrospective evaluation of pubertal development and linear growth of girls with Turner Syndrome treated with oral and transdermal estrogen

Cakir E. D. P., SAĞLAM H., EREN E., Ozgur T., TARIM Ö. F.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.28, ss.1219-1226, 2015 (SCI-Expanded)

Pediatric patients with pheochromocytoma: Experience of a tertiary health center.

EREN E., SAĞLAM H., Caliskan Y., KIRIŞTIOĞLU İ., Tarim Ö. F.

Pediatrics international : official journal of the Japan Pediatric Society , cilt.57, sa.5, ss.875-9, 2015 (SCI-Expanded)

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group.

Darendeliler F., Yesilkaya E., BEREKET A., Bas F., Bundak R., Sari E., et al.

Journal of clinical research in pediatric endocrinology , cilt.7, sa.3, ss.183-91, 2015 (SCI-Expanded)

Evaluation of late effects of postoperative radiotherapy in patients with medulloblastoma

Karadag O., DEMİRÖZ ABAKAY C., Ozkan L., SAĞLAM H., Demirkaya M.

TURKISH JOURNAL OF PEDIATRICS , cilt.57, sa.2, ss.167-171, 2015 (SCI-Expanded)

Turner syndrome and associated problems in Turkish children: a multicenter study.

Yesilkaya E., BEREKET A., Darendeliler F., Bas F., Poyrazoglu S., Aydin B. K., et al.

Journal of clinical research in pediatric endocrinology , cilt.7, sa.1, ss.27-36, 2015 (SCI-Expanded)

Novel mutation of the electron transferring flavoprotein dehydrogenase (ETFDH) gene in the isolated myopathic form of coenzyme q10 deficiency

Gorukmez O., Gorukmez O., Sag S. O., ERDÖL Ş., Saglam H., Yakut T.

Genetic Counseling , cilt.26, sa.2, ss.259-262, 2015 (SCI-Expanded)

preface Başyazi

Sağlam H., Sapan N.

Guncel Pediatri , cilt.12, sa.3, 2014 (SCI-Expanded)

Evaluation of electrocardiographic parameters for early diagnosis of autonomic dysfunction in children and adolescents with type-1 diabetes mellitus.

Uysal F., Ozboyaci E., Bostan Ö. M., SAĞLAM H., Semizel E., ÇİL E.

Pediatrics international : official journal of the Japan Pediatric Society , cilt.56, sa.5, ss.675-80, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.

Cangul H., SAĞLAM H., Saglam Y., EREN E., Dogan D., Kendall M., et al.

Journal of pediatric endocrinology & metabolism : JPEM , cilt.27, ss.1021-5, 2014 (SCI-Expanded)

Etiological evaluation of adolescents with primary amenorrhea.

EREN E., SAĞLAM H., Cakir E. D. P., Tarim Ö. F.

Indian journal of pediatrics , cilt.81, sa.9, ss.861-5, 2014 (SCI-Expanded)

A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism.

Cangul H., Schoenmakers N. A., SAĞLAM H., Doganlar D., Saglam Y., EREN E., et al.

Journal of pediatric endocrinology & metabolism : JPEM , cilt.27, ss.731-5, 2014 (SCI-Expanded)

Preface

Sağlam H., Sapan N.

Guncel Pediatri , cilt.12, sa.2, 2014 (SCI-Expanded)

Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community.

Cangul H., Aycan Z., Olivera-Nappa A., SAĞLAM H., Schoenmakers N. A., Boelaert K., et al.

Clinical endocrinology , cilt.79, sa.2, ss.275-81, 2013 (SCI-Expanded)

Evaluation of the endocrine functions in pediatric patients with cyanotic congenital heart disease

EREN E., Cakir E. D. P., Bostan O., SAĞLAM H., Tarim Ö. F.

BIOMEDICAL RESEARCH-INDIA , cilt.24, sa.2, ss.211-215, 2013 (SCI-Expanded)

Testicular adrenal rest tumors in patients with congenital adrenal hyperplasia.

Cakir E. D. P., Mutlu F. S., EREN E., Pasa A. O., SAĞLAM H., Tarim Ö. F.

Journal of clinical research in pediatric endocrinology , cilt.4, sa.2, ss.94-100, 2012 (SCI-Expanded)

TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis.

Cangul H., Aycan Z., SAĞLAM H., Forman J. R., Cetinkaya S., Tarim Ö. F., et al.

Journal of pediatric endocrinology & metabolism : JPEM , cilt.25, ss.419-26, 2012 (SCI-Expanded)

Resolution of Autoimmune Oophoritis after Thymectomy in a Myasthenia Gravis Patient

Cakir E. D. P., Ozdemir O., EREN E., SAĞLAM H., Okan M., TARIM Ö. F.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.3, sa.4, ss.212-215, 2011 (SCI-Expanded)

Time-Dependent Alterations in Growth and Bone Health Parameters Evaluated at Different Posttreatment Periods in Pediatric Oncology Patients

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.28, ss.588-599, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

Evaluation of the patients with congenital hypothyroidism: Effect of the national screening program Konjenital Hipotiroidili Olgularin Deǧerlendirilmesi: Ulusal Tarama Programinin Etkisi

EREN E., SAĞLAM H., Zengin A., Gül Y., ÇAKIR E. U., ÖZGÜR T., et al.

Guncel Pediatri , cilt.9, sa.1, ss.28-33, 2011 (SCI-Expanded)

Thyroid Functions in Long-Term Survivors of Pediatric Hodgkin's Lymphoma Treated with Chemotherapy and Radiotherapy

Demirkaya M., Sevinir B. B., Sağlam H., Ozkan L., Akaci O.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.3, ss.89-94, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

The use of complementary and alternative medicine in patients with common variable immunodeficiency.

Karali Y., Saglam H., Karali Z., Kilic S. Ş.

Journal of investigational allergology & clinical immunology , cilt.21, sa.6, ss.480-3, 2011 (SCI-Expanded)

Efficacy of biphosphonates in patients with osteogenesis imperfecta Osteogenezis i̇mperfektalı hastalarda bifosfonatların etkinliǧi

EREN E., Sincar Ş., Cakir E. D. P., SAĞLAM H., Tarim Ö.

Guncel Pediatri , cilt.9, sa.3, ss.122-126, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

Clinical course of hyperprolactinemia in children and adolescents: a review of 21 cases.

EREN E., Yapici S., Cakir E. D. P., Ceylan L. A., SAĞLAM H., Tarim Ö. F.

Journal of clinical research in pediatric endocrinology , cilt.3, sa.2, ss.65-9, 2011 (SCI-Expanded)

A retrospective evaluation of patients with rickets Riketsli olguların retrospektif deǧerlendirilmesi

Ocak M., EREN E., Istanbullu K., SAĞLAM H.

Guncel Pediatri , cilt.9, sa.2, ss.75-78, 2011 (SCI-Expanded)

The efficacy of alendronate in children with secondary osteoporosis Sekonder osteoporozlu çocuklarda alendronat tedavisinin etkinliǧi

SAĞLAM H., EREN E., Çakir E. D. P., Özboyaci E., Özboyaci A., ÖZGÜR T., et al.

Guncel Pediatri , cilt.8, sa.3, ss.86-89, 2010 (SCI-Expanded)

Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism.

Cangul H., Morgan N. V., Forman J. R., SAĞLAM H., Aycan Z., Yakut T., et al.

Clinical endocrinology , cilt.73, sa.5, ss.671-7, 2010 (SCI-Expanded)

Robinow syndrome Robinow sendromu

GÖKALP G., EREN E., YAZICI Z., SAĞLAM H.

Guncel Pediatri , cilt.8, sa.1, ss.44-47, 2010 (SCI-Expanded)

Factors influencing glycemic control in children with type 1 diabetes Tip 1 diyabetli çocuklarda glisemik kontrolü etkileyen faktörler

Çakir S., SAĞLAM H., ÖZGÜR T., EREN E., Tarim Ö.

Guncel Pediatri , cilt.8, sa.1, ss.7-19, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

Assessment of Bone Mineral Density and Risk Factors in Children Completing Treatment for Acute Lymphoblastic Leukemia

Gunes A. M., Can E., SAĞLAM H., Ilcol Y. O., Baytan B.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.32, sa.3, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

Acquired generalized lipodystrophy associated with autoimmune hepatitis and low serum C4 level.

Eren E., Özkan T. B., Çakır E. D. P., Sağlam H., Tarım Ö. F.

Journal of clinical research in pediatric endocrinology , cilt.2, ss.39-42, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

A Rare Cause of Precocious Puberty Hepatoblastoma

Eren E., Demirkaya M., Esra Deniz Ç., Sevinir B. B., Sağlam H., Tarım Ö. F.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.1, sa.6, ss.281-283, 2009 (SCI-Expanded)

Abnormal MRI findings in a patient with persistent hyperinsulinemic hypoglycemia of infancy (PHHI)

EREN E., Cakir E. D. P., SAĞLAM H., Tarim Ö. F.

HORMONE RESEARCH , cilt.72, ss.160, 2009 (SCI-Expanded)

Efficiency of alendronate treatment in children with secondary osteoporosis

EREN E., SAĞLAM H., Cakir E. D. P., Ozboyaci E., Ozboyaci A., Tarim Ö. F.

HORMONE RESEARCH , cilt.72, ss.222, 2009 (SCI-Expanded)

Insulin detemir improves glycemic control and reduces hypoglycemia in children with type 1 diabetes: Findings from the Turkish cohort of the PREDICTIVE™ observational study

Atabek M. E., Pirgon O., Emek S., Acar M., Acarturk G., Adas M., et al.

Pediatric Diabetes , cilt.10, sa.6, ss.401-407, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

A rare cause of precocious puberty: hepatoblastoma.

Eren E., Demirkaya M., Çakır E. D. P., Sevinir B., Sağlam H., Tarım Ö. F.

Journal of clinical research in pediatric endocrinology , cilt.1, ss.281-3, 2009 (SCI-Expanded)

Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients

Poyrazoglu S., Saka N., Bas F., Isguven P., Dogu A., DEMİRCİOĞLU S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.21, sa.8, ss.745-751, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

Hyperprostaglandin E syndrome: use of indomethacin and steroid, and death due to necrotizing enterocolitis and sepsis

Cetinkaya M., Koeksal N., ÖZKAN H., DÖNMEZ O., SAĞLAM H., KIRIŞTIOĞLU İ.

TURKISH JOURNAL OF PEDIATRICS , cilt.50, sa.4, ss.386-390, 2008 (SCI-Expanded)

Pseudopseudohypoparathyroidism: A case report

SAĞLAM H., Yuce N., Tarim Ö. F.

HORMONE RESEARCH , cilt.70, ss.233, 2008 (SCI-Expanded)

Reference values for neonatal thyroid volumes in a moderately iodine-deficient area

Koksal N., Akturk B., Saglam H., Yazici Z., Cetinkaya M.

Journal of Endocrinological Investigation , cilt.31, sa.7, ss.642-646, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

L-thyroxine is effective in decreasing thyroid size in children with simple, diffuse, euthyroid goiter

SAĞLAM H., Karali Y., Karali Z., Tarim Ö. F.

HORMONE RESEARCH , ss.171, 2008 (SCI-Expanded)

Prevalence and correlates of obesity in schoolchildren from the city of Bursa, Turkey.

Sağlam H., Tarım Ö. F.

Journal of clinical research in pediatric endocrinology , cilt.1, ss.80-8, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

The effect of pediatric cancer therapy on growth and bone health

Sevinir B., Kart F., Saglam H., Ilco Y.

PEDIATRIC BLOOD & CANCER , cilt.49, sa.4, ss.552-553, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

Hormonal side effects of interferon-alpha therapy in children with chronic hepatitis B infection

Oezkan T., SAĞLAM H.

TURKISH JOURNAL OF GASTROENTEROLOGY , cilt.18, sa.2, ss.126-128, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

Bilateral multiple pulmonary arteriovenous fistulas and duplicated renal collecting system in a child with Noonan's syndrome.

Semizel E., Bostan Ö. M., Saglam H.

Cardiology in the young , cilt.17, sa.2, ss.229-31, 2007 (SCI-Expanded)

Increased incidence of congenital hypothyroidism due to iodine deficiency

Saglam H., Bukukuysal L., Koksal N., Ercan İ., Tarim Ö. F.

PEDIATRICS INTERNATIONAL , cilt.49, sa.1, ss.76-79, 2007 (SCI-Expanded)

Evaluation of patients with Graves' disease

Poyrazoglu S., Saka N., Bas F., Isguven P., Dogu A., DEMİRCİOĞLU S., et al.

HORMONE RESEARCH , cilt.65, ss.41, 2006 (SCI-Expanded)

Marden-Walker syndrome with some additional anomalies

Ozbek S., Saglam H., Ozdamar E.

PEDIATRICS INTERNATIONAL , cilt.47, sa.1, ss.92-94, 2005 (SCI-Expanded)

Severe hypospadias associated with Robertsonian translocation

Kilic N., Balkan E., Saglam H., Yakut T., Dogruyol H.

UROLOGIA INTERNATIONALIS , cilt.74, sa.4, ss.373-376, 2005 (SCI-Expanded)

Meropenem decreases serum level of valproic acid

Nacarkucuk E., Saglam H., Okan M.

PEDIATRIC NEUROLOGY , cilt.31, sa.3, ss.232-234, 2004 (SCI-Expanded)

Evaluation of the need for routine preoperative latex allergy tests in children

Sapan N., Nacarkucuk E., Canitez Y., Saglam H.

PEDIATRICS INTERNATIONAL , cilt.44, sa.2, ss.157-162, 2002 (SCI-Expanded)

Evaluation of the need for routine preoperative latex allergy tests in children.

Sapan N., Nacarkucuk E., Canitez Y., Saglam H.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.105, sa.1, 2000 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Does Growth Hormone Treatment Advance Bone Age?

Sali E., SAĞLAM H., EREN E., Tarim Ö. F.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.15, sa.2, ss.42-49, 2017 (ESCI)

Retrospective Evaluation of Patients Diagnosed with Osteogenesis Imperfecta

ASLAN M. T., EREN E., SAĞLAM H., Tarim Ö. F.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.15, sa.1, ss.1-5, 2017 (ESCI)

A determination of the quality of life of children and adolescents with type 1 diabetes and their parents

Özyazıcıoğlu N., Avdal E. Ü., Sağlam H.

INTERNATIONAL JOURNAL OF NURSING SCIENCES , cilt.4, sa.2, ss.94-98, 2017 (ESCI) Sürdürülebilir Kalkınma

A Determination of The Quality of children and Adolescent with Type 1 Diabetes and their Parents

Özyazıcıoğlu N., Ünsal Avdal E., Sağlam H.

International Journal of Nursing Science , cilt.4, sa.2, ss.94-98, 2017 (ESCI) Sürdürülebilir Kalkınma

Hipofosfatazya

SAĞLAM H., ERDÖL Ş.

Türkiye Klinikleri Tip Bilimleri Dergisi , cilt.1, sa.1, ss.87-92, 2016 (Scopus)

Evaluation of children presenting with diabetic ketoacidosis Diyabetik ketoasidozla başvuran çocuk olguların değerlendirilmesi

Koyuncu E., SAĞLAM H., Tarim Ö. F.

Guncel Pediatri , cilt.14, sa.3, ss.116-123, 2016 (Scopus) Sürdürülebilir Kalkınma

Kalıtsal metabolik hastalıklara klinik yaklaşım

BÜLBÜL BAŞKAN E., YAZİCİ S., YAZICI ÖZTÜRK Z., SAĞLAM H., SARICAOĞLU H.

Türkiye Klinikleri Tip Bilimleri Dergisi , cilt.1, sa.1, ss.81-86, 2016 (Scopus)

Results of Thyroid Function Tests in Premature Infants

Dogan P., Bagci O., Koksal N., ÖZKAN H., Varal I. G., EREN E., et al.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.14, sa.1, ss.10-17, 2016 (ESCI)

Alström Sendromu

SÖBÜ E., EREN E., SAĞLAM H., TARIM Ö. F.

Turkiye Klinikleri J Case Rep , cilt.24, sa.2, ss.34-37, 2016 (Hakemli Dergi)

A Turkish Patient With Succinyl-CoA:3-Oxoacid CoA Transferase Deficiency Mimicking Diabetic Ketoacidosis

ERDÖL Ş., TURE M., YAKUT T., SAĞLAM H., SASAI H., ABDELKREEM E., et al.

Journal of Inborn Errors of Metabolism Screening , cilt.4, ss.1-5, 2016 (Hakemli Dergi) Sürdürülebilir Kalkınma

Preface Başyazı

Sağlam H., Sapan N.

Guncel Pediatri , cilt.13, sa.3, 2015 (Scopus)

Preface

Saglam H., Sapan N.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.13, sa.3, 2015 (ESCI)

Preface

Saglam H., Sapan N.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.13, sa.2, 2015 (ESCI)

Preface

Saglam H., Sapan N.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.13, sa.1, 2015 (ESCI)

Diagnostic criteria of growth hormone deficiency needs to be reevaluated

Sali E., SAĞLAM H., Tarim Ö.

Guncel Pediatri , cilt.10, sa.3, ss.74-79, 2012 (Scopus)

Efficacy of Biphosphonates in Patients with Osteogenesis Imperfecta

EREN E., Sincar S., Cakir E. D. P., SAĞLAM H., TARIM Ö. F.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.9, sa.3, ss.122-126, 2011 (ESCI) Sürdürülebilir Kalkınma

A Retrospective Evaluation of Patients with Rickets

Ocak M., EREN E., Istanbullu K., SAĞLAM H.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.9, sa.2, ss.75-78, 2011 (ESCI)

Evaluation of the Patients with Congenital Hypothyroidism: Effect of the National Screening Program

EREN E., SAĞLAM H., Zengin A., Gul Y., ÇAKIR E. U., ÖZGÜR T., et al.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.9, sa.1, ss.28-33, 2011 (ESCI)

The efficiency of two-stage technique for proximal hypospadias Proksimal hipospadias onariminda çift seansli Bracka tekniǧinin etkinliǧi

Kaçar M., ÇELİK F., SAĞLAM H., Balkan E., KILIÇ N.

Cocuk Cerrahisi Dergisi , cilt.24, sa.1, ss.18-23, 2010 (Scopus)

The Efficacy of Alendronate in Children with Secondary Osteoporosis

SAĞLAM H., EREN E., Cakir E. D. P., Ozboyaci E., Ozboyaci A., ÖZGÜR T., et al.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.8, sa.3, ss.86-89, 2010 (ESCI)

Factors Influencing Glycemic Control in Children with Type 1 Diabetes

Cakir S., SAĞLAM H., ÖZGÜR T., EREN E., TARIM Ö. F.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.8, sa.1, ss.7-19, 2010 (ESCI) Sürdürülebilir Kalkınma

Robinow Syndrome

GÖKALP G., EREN E., YAZICI Z., SAĞLAM H.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.8, sa.1, ss.44-47, 2010 (ESCI)

Growth hormone deficiency Büyüme hormonu eksikliǧi

Tarim Ö., SAĞLAM H.

Guncel Pediatri , cilt.8, sa.1, ss.36-38, 2010 (Scopus)

Psöriazisli çocuk olguda topikal kortikosteroidin yanlış kullanımı ile gelişen cushing sendromu

Turkiye Klinikleri Journal of Dermatology , cilt.19, sa.4, ss.210-213, 2009 (Hakemli Dergi)

Clinical and Laboratory Characteristics of the Children with Diabetic Ketoacidosis

SAĞLAM H., EREN E., Cakir E. D., Yuce N., Yildiz N., Cakir S., et al.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.6, sa.3, ss.94-98, 2008 (ESCI) Sürdürülebilir Kalkınma

Evaluation of Children with Goiter and Treatment Outcomes

KARALI Y., SAĞLAM H., Kamber K., Karali Z., SIĞIRLI D., TARIM Ö. F.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , sa.1, ss.10-18, 2008 (ESCI) Sürdürülebilir Kalkınma

Evaluation of Endocrine Complications in Patients with Thalassemia Major

Baytan B., Sağlam H., Erdöl Ş., Aysun B., Özgür T., Ünsal G., et al.

The Journal of Current Pediatrics , sa.6, ss.58-65, 2008 (Scopus)

Hormonal side effects of interferon-α therapy in children with chronic hepatitis B infection

ÖZKAN T. M., SAĞLAM H.

Turkish Journal Of Gastroenterology , cilt.18, sa.2, ss.126-128, 2007 (Scopus) Sürdürülebilir Kalkınma

Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mutation at the SOX9 locus

Temel Ş. G., Gulten T., Yakut T., Saglam H., Kilic N., Bausch E., et al.

Sexual Development , cilt.1, sa.1, ss.24-34, 2006 (Scopus)

APECED syndrome in a child with early presentation of type I diabetes mellitus

SAĞLAM H., TARIM Ö. F.

International Pediatrics , cilt.15, sa.3, ss.154-157, 2000 (Scopus)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

TİP 1 DİABETES MELLİTUS VE ÇÖLYAK HASTALIĞI BİRLİKTELİĞİ

BUHUR PİRİMOĞLU M., ŞAHİN K. C., DENKBOY ÖNGEN Y., ARSOY H. A., EREN E., SAĞLAM H., et al.

2. ULUSAL ÇOCUK VE ERGEN DİYABET SEMPOZYUMU, Türkiye, 23 - 25 Aralık 2021 Sürdürülebilir Kalkınma

Ailesel Hipokalsiürik hiperkalsemi: Geniş bir aile serisi

DENKBOY ÖNGEN Y., EREN E., Demirbaş Ö., Orhan G., Topak A., TARIM Ö. F., et al.

16. Ulusal Pediatri Kış Kongresi, Türkiye, 8 - 11 Mart 2020

AİLESEL HİPOKALSİÜRİK HİPERKALSEMİ: GENİŞ BİR AİLE SERİSİ

DENKBOY ÖNGEN Y., EREN E., DEMİRBAŞ Ö., GÖRÜKMEZ O., TOPAK A., Tarım Ö., et al.

16. Ulusal Uludağ Pediatri Kış Kongresi, Bursa, Türkiye, 08 Mart 2020

Lysinuric protein intolerance and HOIP deficiency in a boy: SLCA7A and RNF31 gene disruptions

Aliyeva L., ERDÖL Ş., Gorukmez O., Turkgenc B., GÜRKAN H., Yarali Y., et al.

European Biotechnology Congress, Athens, Yunanistan, 26 - 28 Nisan 2018, cilt.280

Tekrarlayan Kemik Kırıklarının Nadir Bir Nedeni: Piknodizostozis

DENKBOY ÖNGEN Y., DOĞAN D., SÖBÜ E., EREN E., SAĞLAM H., TARIM Ö. F.

11. Uludağ Pediatri Kış Kongresi, Bursa, Türkiye, 15 Mart - 18 Mayıs 2015

Papiller Tiroid Karsinomu Olgularımız: On Yıllık Deneyimden Çıkarımlar.

Demirbaş Ö., Eren E., Gürpınar A. N., Demirkaya M., Saraydaroğlu Ö., Parlak A., et al.

14.uludağ pediatri kış kongresi. 11-14 Mart 2018, Bursa, Türkiye, 11 - 14 Mart 2018

Lysinuric protein intolerance and HOIP deficiency in a boy with homozygous missense mutation in the RNF31 gene and homozygous deletion of SLC7A7 gene

ALİYEVA L., ERDÖL Ş., GÖRÜKMEZ O., GÜRKAN H., KARALI Y., BAYTAN B., et al.

Erciyes Tıp Genetik Günleri, Kayseri, Türkiye, 7 - 10 Mart 2018

Transferrin glikoformları referans aralıklarının pediyatrik yaş gruplarına göre düzenlenmesi

Bozyiğit C., Yılmaztepe Oral A., Özkaya G., Sağlam H., Erdöl Ş., Dirican M.

KBUD Kongre Lab Expo, 1 - 05 Ekim 2017

CLINICAL AND LABORATORY CHARACTERISTICS OF HYPERPROLACTINEMIC CHILDREN AND ADOLESCENTS: NATIONAL SURVEY.

EREN E., ERGÜR A., İŞGÜVEN Ş. P., ÇELEBİ BİTKİN E., BERBEROĞLU M., ŞIKLAR Z., et al.

IMPE 2017, 14 - 17 Eylül 2017 Sürdürülebilir Kalkınma

Evaluation of a Case With Niemann-Pick Type C Under Miglustat Therapy

ICIEM 2017, Rio de Janeiro, Brezilya, 5 - 08 Eylül 2017

A rare cause of isolated hepatomegaly:Glycogen-storage disease type VI

ICIEM 2017, 5 - 08 Eylül 2017

A Rare Form of GM1-Gangliosidosis:The Late Infantile Variant

ICIEM 2017, Rio de Janeiro, Brezilya, 5 Ağustos - 08 Eylül 2017

Türk Hipofosfatazyalı Olguların Klinik ve Genetik Bulguları

ÇEKİÇ Ş., SAĞLAM H., Görükmez O., TARIM Ö. F., KILIÇ GÜLTEKİN S. Ş.

XIV. Ulusal Metabolik Hastalıklar ve Beslenme Kongresi, BODRUM, Türkiye, 26 - 30 Nisan 2017

MUKOPOLİSAKKARİDOZ OLGULARINDA KARDİYAK BULGULAR

ERDÖL Ş., UYSAL F., DORUM S., BOSTAN Ö. M., SAĞLAM H.

V. ULUSLARARASI KATILIMLI LİZOZOMAL HASTALIKLAR KONGRESİ, Muğla, Türkiye, 14 - 17 Nisan 2017

HAX 1 Mutasyonu Olan Olguların Pubertal Gelişim ve Gonadal Foksiyonlarının Değerlendirilmesi Endikasyon Dışı İlaç Kullanım Talep Formu

ÇEKİÇ Ş., SAĞLAM H., Görükmez O., YAKUT T., TARIM Ö. F., KILIÇ GÜLTEKİN S. Ş.

23. ULUSAL ALERJİ VE KLİNİK İMMUNOLOJİ KONGRESİ, Türkiye, 8 - 12 Ekim 2016

HAX-1 Mutasyonu Olan Hastalarda Pubertal GelişiminDeğerlendirilmesi

23. Ulusal Alerji ve Klinik İmmünoloji Kongresi, Türkiye, 8 - 12 Ekim 2016

Delayed puberty and gonadal failure in patients with HAX 1 mutation

ÇEKİÇ Ş., saglam H., tarim o., KILIÇ GÜLTEKİN S. Ş.

ICI, 21 Ağustos 2016, cilt.46, ss.1-1274

Canakinumab Rezistan Mevalonat Kinaz Eksikliği Bir Olgu Sunumu

ERDÖL Ş., ÇEKİÇ Ş., ÇAKI KILIÇ S., SAĞLAM H., KILIÇ GÜLTEKİN S. Ş.

3. Çocuk Romatoloji Kongresi, Türkiye, 21 - 24 Nisan 2016

Kromhidrozisli Olgularımız

ERDÖL Ş., KARAKAYA S., DORUM S., SAĞLAM H.

12. Uludağ Pediatri Kış Kongresi, Bursa, Türkiye, 13 - 16 Mart 2016

Büyüme ve Nöromotor Gerilik İle Başvuran Prader Willi Sendromu

12. ULUDAĞ PEDİATRİ KIŞ KONGRESİ, Bursa, Türkiye, 13 - 16 Mart 2016

Nadir Bir Olgu Nedeniyle Ornitin Amino Transferaz Eksikliği

12. ULUDAĞ PEDİATRİ KIŞ KONGRESİ, Bursa, Türkiye, 13 - 16 Mart 2016

Reye-Benzeri Sendromun Nadir Bir Nedeni 3-Metilkrotonil Karboksilaz Eksikliği

ERDÖL Ş., DORUM S., ŞAHİN N. Ü., ÖZGÜR T., SAĞLAM H., ÖZKAN T. M.

12. ULUDAĞ PEDİATRİ KIŞ KONGRESİ, Bursa, Türkiye, 13 - 16 Mart 2016

Konjenital Hipotiroidi ve Biyotinidaz Eksikliği Birlikteliği

ERDÖL Ş., DORUM S., SÖBÜ E., EREN E., SAĞLAM H., TARIM Ö. F.

12. ULUDAĞ PEDİATRİ KIŞ KONGRESİ, Bursa, Türkiye, 13 - 16 Mart 2016

Miglustat treatment in an early infantile form of GM1gangliosidosis

SSIEM 2015 Annual Symposium, Lyon, Fransa, 1 - 04 Eylül 2015, cilt.38, ss.268

Treatment experience in a patient with serious mevalonicaciduria

ERDÖL Ş., ÇEKİÇ Ş., DORUM S., Cakı S., SAĞLAM H., kılıc s. s.

SSIEM 2015 Annual Symposium, Lyon, Fransa, 1 - 04 Eylül 2015, cilt.38, ss.233

Metabolic group study for consensus development on themanagement of phenylketonuria

BALCI M. C., DEMİRKOL M., Ozer I., Aktuglu C., SAĞLAM H., CESUR Y., et al.

SSIEM 2015 Annual Symposium, Lyon, Fransa, 01 Eylül 2015, cilt.38, ss.349

A novel mutation in a patient with early infantile type GM1 gangliosidosis

SSIEM 2015 Annual Symposium, Lyon, Fransa, 1 - 04 Eylül 2015, cilt.38, ss.369

Kalıtsal Metabolik Hastalıklarda Göz Dibi Muayenesinin Önemi- 11. Uludağ Pediatri Kış Kongresi 15 – 18 Mart 2015

ERDÖL Ş., DORUM S., BODUR M., OKAN M. S., SAĞLAM H.

11. Uludağ Pediatri Kış Kongresi, Türkiye, 15 Mart - 18 Mayıs 2015

Hipoglisemi ve Trombositopeni ile Gelen Glikojen Depo Hastalığı Tip IV Olgusu

ERDÖL Ş., TURE M., DORUM S., YAKUT T., SAĞLAM H.

XIII. Ulusal Metabolik Hastalıklar ve Beslenme Kongresi, Adana, Türkiye, 14 - 18 Nisan 2015

Sağlık Bakanlığı Ulusal Neonatal Tarama Programı ile Başvuran GM1-Gangliosidozis Olgusu

XIII. Ulusal Metabolik Hastalıklar ve Beslenme Kongresi, Adana, Türkiye, 14 - 18 Nisan 2015

Klasik Fenilketonüri Tanısıyla İzlenen GTPCH Eksikliği Olgusu