Results 131 to 140 of about 2,517,817 (182)

Bilateral diabetic Charcot neuroarthropathy of the knee in a young woman with diabetes suspected of Wolfram-like syndrome. [PDF]

Diabetol Int
Jojima T, Iijima T, Sagara M, Suda K, Saito M, Tanuma D, Sakurai S, Tomaru T, Yamaguchi Y, Usui I, Taneichi H, Aso Y.   +11 more
europepmc   +1 more source

Adiponectin and leptin levels in mothers, fetuses, and neonates with intrauterine growth restriction compared to those with appropriate gestational age. [PDF]

Front Endocrinol (Lausanne)
Parveen N, Iqbal N, Mohamed AAA, Shahid SMA, Abdalla RAH, Elhussein GEMO, Azhar MA, Saleem M, Khan MS.   +8 more
europepmc   +1 more source

Evaluating the use of GLP-1 receptor agonists in Wolfram syndrome patients. [PDF]

Front Endocrinol (Lausanne)
Lee LA, Tang AF, Asako AE, Ning SF, Reed HA, Duncan E, Lugar HM, Hoekel J, Marshall BA, Hershey T, Urano F.   +10 more
europepmc   +1 more source

Unilateral Retinitis Pigmentosa, Glial Tissue Abnormality, and Microphthalmia in a Young Female Patient: A Case Report. [PDF]

Cureus
Bivona L, Rama T, Wolfe GJ, Maris PJ, Lopez R.   +4 more
europepmc   +1 more source

Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families. [PDF]

Biomolecules
El Fizazi K, Ghaffar A, Bouguenouch L, Saleem IB, Ouldim K, Ahmed ZM, Ridal M, Riazuddin S.   +7 more
europepmc   +1 more source

Type 2 Diabetes Mellitus or Maturity Onset Diabetes in the Young Due to Wolfram Syndrome Gene-1 Mutation-A Perplexing Case. [PDF]

AACE Endocrinol Diabetes
Sharma PP.
europepmc   +1 more source

The Genetic Landscape and Precision Medicine in Neonatal Diabetes Mellitus: From Molecular Mechanisms to Clinical Management. [PDF]

Curr Issues Mol Biol
Meng Y, Zhu L, Dong G, Tang C.
europepmc   +1 more source

Rare Variants in NEUROD1 and PDX1 Are Low-Penetrance Causes of MODY, Whereas Those in APPL1 and WFS1 Are Not Associated With MODY. [PDF]

Diabetes
Sriram A, Wakeling MN, Hattersley AT, Weedon MN, Colclough K, Laver TW, Patel KA.   +6 more
europepmc   +1 more source

Consensus Recommendations for the Clinical Management of Wolfram syndrome Using a Delphi Method

Elliott J, Ahmadi S, Yu-Wai-Man P, Gladstone S, Gebel S, Lynch T, Barrett T, Urano F, International Wolfram Syndrome Clinical Guidelines Consortium.   +8 more
europepmc   +1 more source

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A novel nonsense mutation in the WFS1 gene causes the Wolfram syndrome

Journal of Pediatric Endocrinology and Metabolism, 2016
AbstractWolfram syndrome is a rare autosomal recessive neurodegenerative disorder, which is mostly caused by mutations in ...
Shahab Noorian
exaly   +3 more sources