LBODP030 A Rare Case Of Partial Lipodystrophy From Mpdl (mandibular Hypoplasia, Deafness, Progeroid, Lipodystrophy Syndrome) Due To Pold1 Gene Mutation
Majumdar, Sujoyeeta, Gaba, Ruchi, Ram, Nalini, Force, Bahar Kapoor
Published in Journal of the Endocrine Society (01.11.2022)
Published in Journal of the Endocrine Society (01.11.2022)
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Abstract #1205: An Unusual Case of Pheochromocytoma Secreting Acth Resulting in Cushing Syndrome
Majumdar, Sujoyeeta, Internal Medicine, Moturi, Hemlata, Endocrinology
Published in Endocrine practice (01.05.2015)
Published in Endocrine practice (01.05.2015)
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