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40 in total

1. Magnesium disorders: clinical experience and review of the literature.

Authors: Maria Laura De Feo
Journal: Clin Cases Miner Bone Metab Date: 2009-09

2. Hypomagnesaemic tetany.

Authors: I J Ramage; M Ray; R D Paton; R W Logan; T J Beattie
Journal: J Clin Pathol Date: 1996-04 Impact factor: 3.411

3. Primary hypomagnesemia. I. Absorption Studies.

Authors: I Lombeck; F Ritzl; H G Schnippering; H Michael; H J Bremer; L E Feinendegen; W Kosenow
Journal: Z Kinderheilkd Date: 1975

Review 4. Molecular basis of epithelial Ca2+ and Mg2+ transport: insights from the TRP channel family.

Authors: Henrik Dimke; Joost G J Hoenderop; René J M Bindels
Journal: J Physiol Date: 2010-11-01 Impact factor: 5.182

5. Mild hypotonia and recurrent seizures in an 8-month-old boy: Answers.

Authors: Sare Gülfem Özlü; Cigdem Seher Kasapkara; Serdar Ceylaner; Meryem Erat Nergız; Başak Alan; Songül Yılmaz; Ayşegül Neşe Çıtak Kurt
Journal: Pediatr Nephrol Date: 2019-03-22 Impact factor: 3.714

6. Pathogenesis of hypocalcemia in primary hypomagnesemia: normal end-organ responsiveness to parathyroid hormone, impaired parathyroid gland function.

Authors: S M Suh; A H Tashjian; N Matsuo; D K Parkinson; D Fraser
Journal: J Clin Invest Date: 1973-01 Impact factor: 14.808

Primary hypomagnesemia with secondary hypocalcemia in an infant.

1. Magnesium disorders: clinical experience and review of the literature.

2. Hypomagnesaemic tetany.

3. Primary hypomagnesemia. I. Absorption Studies.

Review 4. Molecular basis of epithelial Ca2+ and Mg2+ transport: insights from the TRP channel family.

5. Mild hypotonia and recurrent seizures in an 8-month-old boy: Answers.

6. Pathogenesis of hypocalcemia in primary hypomagnesemia: normal end-organ responsiveness to parathyroid hormone, impaired parathyroid gland function.

Review 7. Essential role for TRPM6 in epithelial magnesium transport and body magnesium homeostasis.

Review 8. Molecular determinants of magnesium homeostasis: insights from human disease.

9. Familial hypomagnesaemia with secondary hypocalcaemia.

Review 10. Genetic causes of hypercalciuric nephrolithiasis.