Identification of a Novel Homozygous Missense Mutation in the CLDN16 Gene to Decipher the Ambiguous Clinical Presentation Associated with Autosomal Dominant Hypocalcaemia and Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in an Indian Family
Thapa, Rupesh, Roy, Amaresh, Nayek, Kaustav, Basu, Anupam
Published in Calcified tissue international (01.02.2024)
Published in Calcified tissue international (01.02.2024)
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Journal Article
L-Serine Biosynthesis Defect: A Treatable Condition Masquerading as TORCH Infection
Gowda, Vykuntaraju K, Roy, Amaresh, Kinhal, Uddhava, Srinivasan, Varunvenkat M
Published in Indian journal of pediatrics (31.05.2024)
Published in Indian journal of pediatrics (31.05.2024)
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Journal Article
Familial hypomagnesemia with hypercalciuria with nephrocalcinosis: a rare case report
Roy, Amaresh, Laha, Sumanta, Saren, Susama
Published in International journal of research in medical sciences (29.01.2022)
Published in International journal of research in medical sciences (29.01.2022)
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Journal Article