Detalhe da pesquisa
1.
Management and clinical outcomes of patients with homozygous familial hypercholesteremia in Saudi Arabia.
Monaldi Arch Chest Dis
; 93(4)2023 Feb 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36786168
2.
Case report: familial hypocalciuric hypercalcemia.
AME Case Rep
; 8: 55, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38711891
3.
Modern approaches to the management of homozygous familial hypercholesterolemia in the Middle East and North Africa.
J Clin Lipidol
; 18(2): e132-e141, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38158247
4.
Munchausen syndrome by proxy: a case report.
J Med Case Rep
; 17(1): 148, 2023 Apr 04.
Artigo
Inglês
| MEDLINE | ID: mdl-37013583
5.
Surgical management of neonatal severe hyperparathyroidism.
Ann Saudi Med
; 43(6): 352-356, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37916585
6.
CYP3A4 Mutation Causes Vitamin D-Dependent Rickets Type 3: A Case Report in Saudi Arabia.
Cureus
; 15(12): e49976, 2023 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-38179381
7.
Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome.
Horm Res Paediatr
; 88(2): 119-126, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28743110
8.
Persistent hyperinsulinaemic hypoglycaemia of infancy in 43 children: long-term clinical and surgical follow-up.
Asian J Surg
; 29(3): 207-11, 2006 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-16877227
9.
Identification and Treatment of Patients with Homozygous Familial Hypercholesterolaemia: Information and Recommendations from a Middle East Advisory Panel.
Curr Vasc Pharmacol
; 13(6): 759-70, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26311574
10.
Hereditary 1,25-dihydroxyvitamin D resistant rickets due to a mutation causing multiple defects in vitamin D receptor function.
Endocrinology
; 145(11): 5106-14, 2004 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-15308610
11.
Wolcott-Rallison syndrome in two siblings with isolated central hypothyroidism.
Am J Med Genet
; 111(2): 187-90, 2002 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-12210348
12.
Long-term follow up of carbonic anhydrase II deficiency syndrome.
Saudi Med J
; 23(1): 25-9, 2002 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-11938359
13.
Persistent hyperinsulinemic hypoglycemia of infancy in 38 children.
Saudi Med J
; 24(8): 890-4, 2003 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-12939679
14.
Prevalence and characteristics of celiac disease in type I diabetes mellitus in Saudi Arabia.
Saudi Med J
; 24(10): 1113-5, 2003 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-14578980
15.
The syndrome of septo-optic dysplasia in Saudi children.
Saudi Med J
; 25(11): 1675-8, 2004 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-15573200
16.
Spontaneous recovery of propylthiouracil-induced fulminant hepatic failure in an 8-year old child.
Saudi Med J
; 28(5): 804-6, 2007 May.
Artigo
Inglês
| MEDLINE | ID: mdl-17457460
17.
Multiple daily insulin regimen using insulin glargine in type 1 diabetic Saudi children.
Saudi Med J
; 27(2): 262-4, 2006 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-16501691
18.
Continuous subcutaneous insulin infusion in type 1 diabetic Saudi children: a comparison with multiple daily insulin injections.
Ann Saudi Med
; 26(4): 327-8, 2006.
Artigo
Inglês
| MEDLINE | ID: mdl-16891848
19.
Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy.
Ann Saudi Med
; 26(5): 405, 2006.
Artigo
Inglês
| MEDLINE | ID: mdl-17120382
20.
Gender identity in congenital adrenal hyperplasia secondary to 11-hydroxylase deficiency.
Ann Saudi Med
; 26(3): 239-41, 2006.
Artigo
Inglês
| MEDLINE | ID: mdl-16861857