4 results for Fariduddin M.

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A Novel Mutation in FGF23 Causing Severe Manifestation of Hyperphosphataemic Familial Tumoral Calcinosis
American Journal of Medical Case Reports. 2018, 6(5), 99-102. DOI: 10.12691/ajmcr-6-5-6
Pub. Date: June 21, 2018Views: 3444Downloads: 2450
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Bartter Syndrome: A Rare Renal Tubulopathy Presenting with Polyuria, Generalized Weakness and Recurrent Tetany in an Adolescent Male
American Journal of Medical Case Reports. 2018, 6(7), 124-127. DOI: 10.12691/ajmcr-6-7-1
Pub. Date: July 28, 2018Views: 2039Downloads: 1359
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Cyclic Cushing Syndrome, an Enigma in Diagnosis- A Case Report
American Journal of Medical Case Reports. 2016, 4(2), 65-70. DOI: 10.12691/ajmcr-4-2-9
Pub. Date: March 11, 2016Views: 10635Downloads: 8638
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Laron Syndrome: Siblings with Extreme Short Stature and Very High Growth Hormone
American Journal of Medical Case Reports. 2016, 4(6), 198-203. DOI: 10.12691/ajmcr-4-6-4
Pub. Date: June 13, 2016Views: 11065Downloads: 9162
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