Hereditary renal tubular disorders in Turkey: demographic, clinical, and laboratory features
CLINICAL AND EXPERIMENTAL NEPHROLOGY, cilt.15, sa.1, ss.108-113, 2011 (SCI-Expanded, Scopus)
- 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
- Akdeniz 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).