Hereditary renal tubular disorders in Turkey: demographic, clinical, and laboratory features

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Atıf İçin Kopyala

TOPALOĞLU R., Baskin E., BAHAT ÖZDOĞAN E., KAVUKÇU S., Cakar N., DÖNMEZ O., ...Daha Fazla

CLINICAL AND EXPERIMENTAL NEPHROLOGY, cilt.15, sa.1, ss.108-113, 2011 (SCI-Expanded)

• Yayın Türü: Makale / Tam Makale
• Cilt numarası: 15 Sayı: 1
• Basım Tarihi: 2011
• Doi Numarası: 10.1007/s10157-010-0367-z
• Dergi Adı: CLINICAL AND EXPERIMENTAL NEPHROLOGY
• Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Sayfa Sayıları: ss.108-113
• Anahtar Kelimeler: Bartter's syndrome, Cystinosis, Demography, dRTA, Failure to thrive, Features, Gitelman's syndrome, Hereditary renal tubular disorders, Prevalence, pRTA, ACIDOSIS, MUTATIONS, DEAFNESS
• Bursa Uludağ Üniversitesi Adresli: Evet

Özet

The Turkish Renal Tubular Disorders Working Group aimed to form a patient registry database and gathered demographic, clinical, and laboratory data in various hereditary renal tubular disorders (HRTDs).