E-LIB Suche - Ergebnisse für: Al Mutair, Angham N

1

Heterogeneity in Phenotype of Usher-Congenital Hyperinsulin..:

Al Mutair, Angham N. ; Brusgaard, Klaus ; Bin-Abbas, Bassam...
Diabetes Care. 36 (2013) 3 - p. 557-561 , 2013

2

Mutation of theCYP2R1Vitamin D 25-Hydroxylase in a Saudi Ar..:

Al Mutair, Angham N. ; Nasrat, Ghada H. ; Russell, David W.
The Journal of Clinical Endocrinology & Metabolism. 97 (2012) 10 - p. E2022-E2025 , 2012

Link: https://doi.org/10.1210/..

3

Heterogeneity in Phenotype of Usher-Congenital Hyperinsulin..:

Al Mutair, Angham N ; Brusgaard, Klaus ; Bin-Abbas, Bassam...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3579360. , 2013

Link: http://www.ncbi.nlm.nih...

4

Mutation of the CYP2R1 Vitamin D 25-Hydroxylase in a Saudi ..:

Al Mutair, Angham N ; Nasrat, Ghada H ; Russell, David W
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462929. , 2012

Link: http://www.ncbi.nlm.nih...

5

Subclinical Neuropathy in Children With Type I Diabetes Mel..:

Altuwaijri, Waleed A ; Almutair, Angham N ; AlAlwan, Ibrahim A..
Cureus. , 2022

Link: https://doi.org/10.7759/..

6

Patients' Perception of the Use of the EasyPod™ Growth Horm..:

Deeb, Asma ; Al Yaarubi, Saif ; Abbas, Bassam Bin...
Frontiers in Pediatrics. 10 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

7

Second Arab Society for Pediatric Endocrinology and Diabete..:

Deeb, Asma ; Tfayli, Hala ; Hassan, Mona...
Ibnosina Journal of Medicine and Biomedical Sciences. 7 (2015) 3 - p. 61-126 , 2015

Link: https://doi.org/10.4103/..

8

Variable phenotype in five patients with Wolcott-Rallison s..:

Al-Shawi, Manal ; Al Mutair, Angham ; Ellard, Sian.
Journal of Pediatric Endocrinology and Metabolism. 26 (2013) 7-8 - p. , 2013

Link: https://doi.org/10.1515/..

9

Newborn with Dilated Cardiomyopathy Secondary to Vitamin D ..:

Al Azkawi, Hanan ; Al Mutair, Angham
Case Reports in Pediatrics. 2012 (2012) - p. 1-5 , 2012

Link: https://doi.org/10.1155/..

10

Puberty Onset among Boys in Riyadh, Saudi Arabia:

Alwan, Ibrahim Al ; Felimban, Naila ; Altwaijri, Yasmin...
Clinical Medicine Insights: Pediatrics. 4 (2010) - p. CMPed.S4610 , 2010

Link: https://doi.org/10.4137/..

11

Wolcott-Rallison Syndrome Is the Most Common Genetic Cause ..:

Rubio-Cabezas, Oscar ; Patch, Ann-Marie ; Minton, Jayne A. L....
The Journal of Clinical Endocrinology & Metabolism. 94 (2009) 11 - p. 4162-4170 , 2009

Link: https://doi.org/10.1210/..

12

Hypoparathyroidism–retardation–dysmorphism (HRD) syndrome i..:

Al Tawil, Khalil ; Shataiwi, Adnan ; Mutair, Angham..
American Journal of Medical Genetics Part A. 135A (2005) 2 - p. 200-201 , 2005

Link: https://doi.org/10.1002/..

13

Genetic and diabetic auto-antibody markers in Saudi childre..:

Manan, Hakbany ; Angham, Al Mutair ; Sitelbanat, Awadalla
Human Immunology. 71 (2010) 12 - p. 1238-1242 , 2010

Link: https://doi.org/10.1016/..

14

Epidemiology of nutritional rickets in Saudi children:

Al-Atawi, Mohsen ; Al-Mutair, Angham ; Al-Alwan, Ibrahim..
Bone. 43 (2008) - p. S71-S72 , 2008

Link: https://doi.org/10.1016/..

15

Saudi Nursing Students Experience of Distance Learning (e-l..:

Barnawi, Najla A. ; Al-Mutair, Angham ; Al-Ghadeer, Hind
International Journal of Innovative Research in Medical Science. 6 (2021) 3 - p. 212-218 , 2021

Link: https://doi.org/10.23958..