Literature DB >> 5071957

Decreased bicarbonate threshold and renal magnesium wasting in a sibship with distal renal tubular acidosis. (Evaluation of the pathophysiological role of parathyroid hormone).

M F Michelis, A L Drash, L G Linarelli, F R De Rubertis, B B Davis.   

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Year:  1972        PMID： 5071957     DOI： 10.1016/0026-0495(72)90025-x

Source DB:  PubMed          Journal:  Metabolism        ISSN： 0026-0495            Impact factor:   8.694


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  25 in total

1.  Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations.

Authors:  Astrid Godron; Jérôme Harambat; Valérie Boccio; Anne Mensire; Adrien May; Claire Rigothier; Lionel Couzi; Benoit Barrou; Michel Godin; Dominique Chauveau; Stanislas Faguer; Marion Vallet; Pierre Cochat; Philippe Eckart; Geneviève Guest; Vincent Guigonis; Pascal Houillier; Anne Blanchard; Xavier Jeunemaitre; Rosa Vargas-Poussou
Journal:  Clin J Am Soc Nephrol       Date:  2012-03-15       Impact factor: 8.237

2.  Phosphorylated claudin-16 interacts with Trpv5 and regulates transcellular calcium transport in the kidney.

Authors:  Jianghui Hou; Vijay Renigunta; Mingzhu Nie; Abby Sunq; Nina Himmerkus; Catarina Quintanova; Markus Bleich; Aparna Renigunta; Matthias Tilmann Florian Wolf
Journal:  Proc Natl Acad Sci U S A       Date:  2019-09-05       Impact factor: 11.205

3.  Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations.

Authors:  Ju Hyung Kang; Hyun Jin Choi; Hee Yeon Cho; Joo Hoon Lee; Il Soo Ha; Hae Il Cheong; Yong Choi
Journal:  Pediatr Nephrol       Date:  2005-07-27       Impact factor: 3.714

Review 4.  Pediatric nephrolithiasis: a systematic approach from diagnosis to treatment.

Authors:  Giuseppina Marra; Francesca Taroni; Alfredo Berrettini; Emanuele Montanari; Gianantonio Manzoni; Giovanni Montini
Journal:  J Nephrol       Date:  2018-04-21       Impact factor: 3.902

Review 5.  Inherited and acquired disorders of magnesium homeostasis.

Authors:  Matthias Tilmann Florian Wolf
Journal:  Curr Opin Pediatr       Date:  2017-04       Impact factor: 2.856

Review 6.  Hereditary causes of kidney stones and chronic kidney disease.

Authors:  Vidar O Edvardsson; David S Goldfarb; John C Lieske; Lada Beara-Lasic; Franca Anglani; Dawn S Milliner; Runolfur Palsson
Journal:  Pediatr Nephrol       Date:  2013-01-20       Impact factor: 3.714

7.  CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Authors:  Martin Konrad; Jianghui Hou; Stefanie Weber; Jörg Dötsch; Jameela A Kari; Tomas Seeman; Eberhard Kuwertz-Bröking; Amira Peco-Antic; Velibor Tasic; Katalin Dittrich; Hammad O Alshaya; Rodo O von Vigier; Sabina Gallati; Daniel A Goodenough; André Schaller
Journal:  J Am Soc Nephrol       Date:  2007-11-14       Impact factor: 10.121

Review 8.  Genetics of hereditary disorders of magnesium homeostasis.

Authors:  Karl P Schlingmann; Martin Konrad; Hannsjörg W Seyberth
Journal:  Pediatr Nephrol       Date:  2003-11-22       Impact factor: 3.714

9.  Renal magnesium wasting, incomplete tubular acidosis, hypercalciuria and nephrocalcinosis in siblings.

Authors:  F Manz; K Schärer; P Janka; J Lombeck
Journal:  Eur J Pediatr       Date:  1978-06-20       Impact factor: 3.183

10.  Pathophysiology of the renal acidification defect present in the syndrome of familial hypomagnesaemia-hypercalciuria.

Authors:  J Rodríguez-Soriano; A Vallo
Journal:  Pediatr Nephrol       Date:  1994-08       Impact factor: 3.714
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