A boy with Prader-Willi syndrome: unmasking precocious puberty during growth hormone replacement therapy

Obesity and Bariatric SurgeryThyroid

Congenital hypothyroidism due to ectopic sublingual thyroid gland in Prader-Willi Syndrome: a case report

Ital J Pediatr.

Bocchini S, Fintini D, Grugni G, Boiani A, Convertino A, Crinò A

doi: 10.1186/s13052-017-0403-7.

Obesity and Bariatric Surgery

Laparoscopic sleeve gastrectomy in an adolescent with Prader-Willi syndrome: psychosocial implications

Nutrition.

Martinelli V, Chiappedi M, Pellegrino E, Zugnoni M, Caccialanza R, Muggia C, Cogni G, Chiovato L, Bichisao G, Politi P, Pietrabissa A, Peri A

doi: 10.1016/j.nut.

Thyroid

Case Report: A Case of Pituitary Adenoma Producing Growth Hormone and Thyroid-Stimulating Hormone Simultaneously

Front Endocrinol (Lausanne)

Sanada J, Tatsumi F, Kamei S, Fushimi Y, Shimoda M, Kohara K, Nakanishi S, Kaku K, Mune T, Kaneto H

doi: 10.3389/fendo.2021.659076

Further Publications

Case Report: Lipoma of the Tuber Cinereum Mimicking a Pituitary Gland Abnormality in a Girl With Central Precocious Puberty

Front Endocrinol (Lausanne)

Giacomozzi C, Nicolì L, Sozzi C, Piovan E, Maghnie M

doi: 10.3389/fendo.2021.766253

Further Publications

Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) and Subsequent Central Diabetes Insipidus: A Rare Presentation of Pituitary Apoplexy

Case Rep Endocrinol.

Smedegaard SB, Jørgensen JO, Rittig N

doi: 10.1155/2019/7592648.

Obesity and Bariatric Surgery

Case Report: Liraglutide for Weight Management in Beckwith-Wiedemann Syndromic Obesity

Front Endocrinol (Lausanne)

Caputo M, Daffara T, Bellone S, Mancioppi V, Marzullo P, Aimaretti G, Prodam F

doi: 10.3389/fendo.2021.687918

Thyroid

Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation

Front Endocrinol (Lausanne).

Majdoub H, Amselem S, Legendre M, Rath S, Bercovich D, Tenenbaum-Rakover Y

doi: 10.3389/fendo.2019.00381.

Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report

BMC Nephrol.

Awanami Y, Fukuda M, Nonaka Y, Takashima T, Matsumoto K, Yamasaki M, Miyazono M, Ikeda Y

doi: 10.1186/

Diabetes - General

Rituximab for the treatment of type B insulin resistance syndrome: a case report and review of the literature

Diabet Med.

Iseri K, Iyoda M, Shikida Y, Inokuchi T, Morikawa T, Hara N, Hirano T, Shibata T

doi: 10.1111/dme.13524.

Related content

Congenital hypothyroidism due to ectopic sublingual thyroid gland in Prader-Willi Syndrome: a case report

Laparoscopic sleeve gastrectomy in an adolescent with Prader-Willi syndrome: psychosocial implications

Case Report: A Case of Pituitary Adenoma Producing Growth Hormone and Thyroid-Stimulating Hormone Simultaneously

Case Report: Lipoma of the Tuber Cinereum Mimicking a Pituitary Gland Abnormality in a Girl With Central Precocious Puberty

Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) and Subsequent Central Diabetes Insipidus: A Rare Presentation of Pituitary Apoplexy

Case Report: Liraglutide for Weight Management in Beckwith-Wiedemann Syndromic Obesity

Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation

Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report

Rituximab for the treatment of type B insulin resistance syndrome: a case report and review of the literature