Detalhe da pesquisa
1.
Letter to the Editor: MAFLD versus MASLD criteria debate- Certainly not for children!
Hepatology
; 2024 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38898579
2.
Expression of CD163 in hereditary gingival fibromatosis: A possible association with TGF-ß1.
J Oral Pathol Med
; 47(3): 286-292, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29325232
3.
Extended clinical features associated with novel Glis3 mutation: a case report.
BMC Endocr Disord
; 17(1): 14, 2017 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28253873
4.
Premature atherosclerosis in children with beta-thalassemia major: New diagnostic marker.
BMC Pediatr
; 17(1): 69, 2017 03 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28279156
5.
First report of acute lymphoblastic leukemia in an Egyptian child with ß-thalassemia major.
Hemoglobin
; 39(2): 127-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25707677
6.
Abdominal mystery in a neonate.
Arch Dis Child Educ Pract Ed
; 105(4): 227-229, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31302593
7.
Unraveling Alström syndrome: Homozygous mutation c.2729C>G in ALMS1 gene across an extended family.
Mol Genet Genomic Med
; 12(1): e2314, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37937857
8.
"Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN2 gene".
Mol Genet Genomic Med
; 12(1): e2282, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37800653
9.
Late onset neonatal sepsis: Can plasma gelsolin be a promising diagnostic marker?
Medicine (Baltimore)
; 103(10): e37356, 2024 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38457556
10.
Down syndrome patients with normal hearts: are they really normal?
Medicine (Baltimore)
; 102(6): e32886, 2023 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36820596
11.
Pediatric myelin oligodendrocyte glycoprotein antibody associated disease-Asymmetric papilledema and elevated ICP are two of the chameleons: A case report.
Medicine (Baltimore)
; 102(8): e32986, 2023 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36827019
12.
An Unusual Case of Headache in a Child: Idiopathic Intracranial Hypertension with Diagnostic Challenge.
Clin Med Insights Case Rep
; 16: 11795476231158509, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36874375
13.
Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation.
Clin Med Insights Endocrinol Diabetes
; 16: 11795514231167059, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37255966
14.
Vertebral artery dissection aneurysm in a pediatric patient: A rare case with unusual clinical manifestations, diagnostic, and management challenges.
Medicine (Baltimore)
; 102(47): e35906, 2023 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38013323
15.
The Study of Carotid Artery Intima-Media Thickness in Children With Epilepsy on Anti-Epileptic Drugs.
Glob Pediatr Health
; 10: 2333794X231200205, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37809362
16.
Beta Thalassemia Carrier Rate: Problem Burden among High School Children.
Curr Pediatr Rev
; 19(2): 203-209, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-35748556
17.
Pediatric sarcoidosis presenting as huge splenomegaly.
Pediatr Int
; 59(3): 366-367, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28317306
18.
The impact of tobacco smoking and electronic cigarette vaping on salivary biomarkers. A comparative study.
Saudi Dent J
; 34(5): 404-409, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35814841
19.
Expression of TGF-ß and MMP-2 in hereditary gingival fibromatosis epithelial cells. A possible contribution of the epithelium to its pathogenesis.
J Oral Biol Craniofac Res
; 12(5): 617-622, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35989975
20.
Novel Melano-Cortin-2-Receptor Gene Mutation Presenting With Infantile Cholestasis: A Case Report.
Clin Med Insights Case Rep
; 15: 11795476221091387, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35418791