Results 191 to 200 of about 8,846 (292)

Mauriac syndrome: a rare complication in patients with type 1 diabetes mellitus. [PDF]

Endocrinol Diabetes Metab Case Rep
Torres JO, Martins DC, Matias AA, Gião N, Dutra E, Malheiro R, Mendes M, Silva-Nunes J.   +7 more
europepmc   +1 more source

Mauriac Syndrome: A Rare Condition With Cushingoid Feature and Hepatomegaly in Poorly Controlled Diabetes Mellitus Type 1. [PDF]

Cureus
Brahmbhatt KJ, Doshi MJ, Dave M, Contractor H, Shah K.   +4 more
europepmc   +1 more source

Muscle pathophysiology and involvement of satellite cells in Pompe disease (glycogenosis type II)

, 2018
Lydie Lagalice
openalex   +1 more source

Pseudoscleroderma concomitant with a muscular glycogenosis of unknown enzymatic defect

, 1972
S. Jabłońska, A Stachów
openalex   +2 more sources

A New Type of Skeletal Muscle Glycogenosis due to Phosphofructokinase Deficiency

, 1965
Mitsuo Nishikawa, Kazuo Tsukiyama, Takumi ENOMOTO, Seiichiro Tarui, Giichi Okuno, Keishi Ueda, Tomoharu IKURA, T Tsujii, Toru Sugase, Masami Suda, Takehiko Tanaka   +10 more
openalex   +2 more sources

Genetic diagnosis of Jordanian patients with glycogen storage diseases. [PDF]

Orphanet J Rare Dis
Shboul M, El-Khateeb M, Fathallah R.
europepmc   +1 more source

Congenital Heart Disease from Infancy to Adulthood: Pathology and Nosology. [PDF]

Biomedicines
Thiene G, Fedrigo M.
europepmc   +1 more source

Inherited metabolic disorders: presentation, clinical types, laboratory diagnosis and genetic markers. [PDF]

Orphanet J Rare Dis
Ijaz A, Abbas S, Shabbir M, Badshah Y, Abid F, Afsar T, Razak S.   +6 more
europepmc   +1 more source

Hepatocellular Ballooning is Due to Highly Pronounced Glycogenosis Potentially Associated with Steatosis and Metabolic Reprogramming. [PDF]

J Clin Transl Hepatol
Ribback S, Peters K, Yasser M, Prey J, Wilhelmi P, Su Q, Dombrowski F, Bannasch P.   +7 more
europepmc   +1 more source

Neuroendocrine cell hyperplasia of infancy: an unusual cause of hypoxemia in children [PDF]

core   +1 more source