Results 131 to 140 of about 22,509 (201)

Case Report: Twenty years of metreleptin therapy in congenital generalized lipodystrophy type 1: the longest reported follow-up to date. [PDF]

Front Endocrinol (Lausanne)
Van der Borght E, Van der Schueren B, Vangoitsenhoven R, Cassiman D, Akinci B, Brown RJ, Oral EA, Mertens A, Martens PJ.   +8 more
europepmc   +1 more source

Lipodystrophy [PDF]

, 2020
openaire   +1 more source

Lipodystrophy and associated factors among patients with diabetes receiving insulin therapy: a multicenter study in Ethiopia. [PDF]

Sci Rep
Bazezew ZA, Zeleke TK, Negesse CT, Mekonnen GB.   +3 more
europepmc   +1 more source

The risk of nephrotic range proteinuria and kidney failure in primary laminopathies is genotype specific. [PDF]

JCI Insight
Sewerin S, Aurnhammer C, Hamed M, Revêchon G, Schönauer R, Findeisen C, Miehle K, Tesařo Vá Š, Georgomanolis T, Bergmann C, Wolff C, Kollár M, Akinci B, Araújo-Vilar D, Ceccarini G, Csajbók É, Gambineri A, Heni M, Scherer T, Štotl I, Sorkina E, Vantyghem MC, Vorona E, Wabitsch M, von Schnurbein J, Vatier C, Roume J, Reznik Y, Eriksson M, Antonin W, Vigouroux C, Halbritter J.   +31 more
europepmc   +1 more source

Genotype-phenotype heterogeneity among patients with lipodystrophy harboring rare POLD1 variants.

J Clin Endocrinol Metab
Hoff FW, Xing C, Huang CY, Simha V, Brown RJ, Garg A.   +5 more
europepmc   +1 more source

Lipodystrophy: an uncommon cause of insulin resistance and young-onset diabetes. [PDF]

JCEM Case Rep
Chaturvedi R, Pradhan A, Kachroo V, Sharma M, Goyal M, Mathew A.   +5 more
europepmc   +1 more source

DICER-driven regulation of lipid metabolism and macrophage-adipocyte crosstalk in partial lipodystrophy. [PDF]

Biomed Pharmacother
Rocha AL, Godoi R, de Lima TI, de Moraes D, Brandão BB, Pinto AFM, Braz-de-Melo HA, da Silva FC, Gonçalves TT, Figueiredo LS, Mazzi JP, de Lima Junior NC, Sousa SML, Miyamoto JE, Leiria LO, Kornfeld JW, Magalhães KG, Moraes-Vieira PM, Saghatelian A, Mori MA.   +19 more
europepmc   +1 more source

Hematopoietic stem cell transplantation-associated partial lipodystrophy. [PDF]

Clin Pediatr Endocrinol
Adachi M.
europepmc   +1 more source

Clinical, genetics and in silico analysis of a novel BSCL2 variant in a patient with CGL2 from Iranian Azeri Turkish ethnic group: expanding the genotypic spectrum through a comparative review. [PDF]

Hum Genome Var
Bazmi H, Jabbarpour N, Asghari AA, Bonaydi M, Motamedi A, Barzegar M.   +5 more
europepmc   +1 more source