Clinical Course and Prognosis of Tubulopathies Characterized by Metabolic Alkalosis in Children
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[1] G. Capasso,et al. Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders. , 2021, Kidney international.
[2] R. Kleta,et al. Inherited Tubulopathies of the Kidney: Insights from Genetics. , 2020, Clinical journal of the American Society of Nephrology : CJASN.
[3] E. Sevinç,et al. SLC26A3 mutation in Turkish neonate and her sibling with congenital chloride diarrhea , 2018, Turk pediatri arsivi.
[4] Zhiying Liu,et al. Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3 , 2019, Endocrine.
[5] R. Kleta,et al. Bartter and Gitelman syndromes: Questions of class , 2019, Pediatric Nephrology.
[6] R. Kleta,et al. Salt-Losing Tubulopathies in Children: What's New, What's Controversial? , 2017, Journal of the American Society of Nephrology : JASN.
[7] R. Kleta,et al. Clinical and diagnostic features of Bartter and Gitelman syndromes , 2017, Clinical kidney journal.
[8] D. Bolignano,et al. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. , 2017, Kidney international.
[9] E. Avner,et al. Renal tubular disorders of electrolyte regulation in children , 2015 .
[10] Brenda R. Hemmelgarn,et al. Notice , 2012, Kidney International Supplements.
[11] M. Buyukcelik,et al. Bartter syndrome and growth hormone deficiency: three cases , 2012, Pediatric Nephrology.
[12] H. Cheong,et al. Genetic basis of Bartter syndrome in Korea. , 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[13] R. Topaloğlu,et al. Hereditary renal tubular disorders in Turkey: demographic, clinical, and laboratory features , 2011, Clinical and Experimental Nephrology.
[14] C. Guyot,et al. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome. , 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[15] Susan L Furth,et al. New equations to estimate GFR in children with CKD. , 2009, Journal of the American Society of Nephrology : JASN.
[16] H. Seyberth. An improved terminology and classification of Bartter-like syndromes , 2008, Nature Clinical Practice Nephrology.
[17] Gülbin Gökçay,et al. Türk çocuklarında vücut ağırlığı, boy uzunluğu, baş çevresi ve vücut kitle indeksi referans değerleri , 2008 .
[18] B. Tönshoff,et al. Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies. , 2002, The American journal of medicine.
[19] J. Gill,et al. Hyperplasia of the Juxtaglomerular Complex with Hyperaldosteronism and Hypokalemic Alkalosis. , 1963 .