17 results on '"Habeb, Abdelhadi M."'
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2. Homozygous Resistance to Thyroid Hormone β: Can Combined Antithyroid Drug and Triiodothyroacetic Acid Treatment Prevent Cardiac Failure?
3. Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ
4. The spectrum of congenital heart diseases in down syndrome
5. An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3)
6. Reduced frequency and severity of ketoacidosis at diagnosis of childhood type 1 diabetes in Northwest Saudi Arabia
7. Does type 1 diabetes mellitus affect bone quality in prepubertal children?
8. Liver Disease and Other Comorbidities in Wolcott-Rallison Syndrome: Different Phenotype and Variable Associations in a Large Cohort
9. Familial glucocorticoid deficiency: a diagnostic challenge during acute illness
10. Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review
11. Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation
12. Permanent neonatal diabetes: different aetiology in Arabs compared to Europeans
13. Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia
14. Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia
15. High incidence of childhood type 1 diabetes in Al-Madinah, North West Saudi Arabia (2004-2009)
16. Response to oral gliclazide in a pre-pubertal child with hepatic nuclear factor-1 alpha maturity onset diabetes of the young
17. Response to Oral Glidazide in a Pre-Pubertal Child with Hepatic Nuclear Factor-1 Alpha Maturity Onset Diabetes of the Young
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