Found: 12
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An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 ( GLIS3).
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 7, p. 1918, doi. 10.1002/ajmg.a.37680
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- Article
Neonatal Adrenal Hematoma with Urinary Tract Infection: Risk Factor or a Chance Association?
- Published in:
- Saudi Journal of Kidney Diseases & Transplantation, 2014, v. 25, n. 2, p. 376, doi. 10.4103/1319-2442.128552
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- Article
Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome.
- Published in:
- Diabetologia, 2018, v. 61, n. 5, p. 1027, doi. 10.1007/s00125-018-4554-x
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- Article
Reduced frequency and severity of ketoacidosis at diagnosis of childhood type 1 diabetes in Northwest Saudi Arabia.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 3, p. 259, doi. 10.1515/jpem-2015-0077
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- Article
Resolving Basal Ganglia Calcification in Hereditary Hypomagnesemia with Secondary Hypocalcemia due to a Novel TRMP6 Gene Mutation.
- Published in:
- Saudi Journal of Kidney Diseases & Transplantation, 2012, v. 23, n. 5, p. 1038, doi. 10.4103/1319-2442.100945
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- Publication type:
- Article
The spectrum of congenital heart diseases in down syndrome.
- Published in:
- Saudi Medical Journal, 2016, v. 37, n. 7, p. 767, doi. 10.15537/smj.2016.7.14536
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- Publication type:
- Article
Liver Disease and Other Comorbidities in Wolcott-Rallison Syndrome: Different Phenotype and Variable Associations in a Large Cohort.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 83, n. 3, p. 190, doi. 10.1159/000369804
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- Article
Ramadan Fasting and Diabetes in Adolescents and Children: A Narrative Review.
- Published in:
- Ibnosina Journal of Medicine & Biomedical Sciences, 2019, v. 11, n. 2, p. 47, doi. 10.4103/ijmbs.ijmbs_21_19
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- Article
Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia.
- Published in:
- Pediatric Diabetes, 2012, v. 13, n. 6, p. 499, doi. 10.1111/j.1399-5448.2011.00828.x
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- Publication type:
- Article
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
- Published in:
- Pediatric Diabetes, 2012, v. 13, n. 4, p. 307, doi. 10.1111/j.1399-5448.2012.00855.x
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- Article
High incidence of childhood type 1 diabetes in Al-Madinah, North West Saudi Arabia (2004-2009)
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- 2011
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- Publication type:
- Journal Article
High incidence of childhood type 1 diabetes in Al-Madinah, North West Saudi Arabia (2004-2009).
- Published in:
- Pediatric Diabetes, 2011, v. 12, n. 8, p. 676, doi. 10.1111/j.1399-5448.2011.00765.x
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- Publication type:
- Article