Naglaa M Kamal
Professor of Pediatrics and Pediatric Hepatology, Pediatric Hepatology Unit, Faculty of Medicine, Cairo University
(email)
Abdominal mystery in a neonate.
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Halabi, A., U. Khan, K. Maazoun, and N. M. Kamal, "Abdominal mystery in a neonate.", Archives of disease in childhood. Education and practice edition, 2019.
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CMV
Case Report: Dubin-Johnson Syndrome Presenting With Infantile Cholestasis: An Overlooked Diagnosis in an Extended Family.
Conventional intensive LED intensive phototherapy oxidative stress burden in neonatal hyperbilirubinaemia of haemolytic origin.
Facial Asymmetry in a Newly Born Baby: Diagnostic Challenge!
First report of SYNE1 arthrogryposis multiplex congenita from Saudi Arabia with a novel mutation: a case report.
Genetic polymorphism of vitamin D receptors and plasminogen activator inhibitor-1 and osteonecrosis risk in childhood acute lymp
IgA Vasculitis Without Typical Skin Rash Concomitated With c-ANCA Positivity.
Infantile Parotid Hemangioma With Diagnostic Dilemma: A Case Report.
Intrafamilial Transmission of Hepatitis C Virus Among Families of Infected Pediatric Oncology Patients.
Knowledge of Neonatal Hyperbilirubinemia Among Primary Health Care Physicians: A Single-Center Experience.
Liver function changes following the introduction of a gluten-free diet in patients with celiac disease.
Novel Melano-Cortin-2-Receptor Gene Mutation Presenting With Infantile Cholestasis: A Case Report.
Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study.
Omega-3 supplementation in children with ADHD and intractable epilepsy
Omega-3 supplementation in children with ADHD and intractable epilepsy
Omega-3 supplementation in children with ADHD and intractable epilepsy
Risk Factors of Intractable Epilepsy in Children with Cerebral Palsy.
Saudi Experts Consensus on Diagnosis and Management of Pediatric Functional Constipation.
VItamin D adolescents
Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients.
endocan
fetus in feto
https://ijn.mums.ac.ir/article_17380.html
https://www.ncbi.nlm.nih.gov/pubmed/26740874
https://www.ncbi.nlm.nih.gov/pubmed/26848373
https://www.ncbi.nlm.nih.gov/pubmed/27330742
https://www.ncbi.nlm.nih.gov/pubmed/27358729
https://www.ncbi.nlm.nih.gov/pubmed/27631238
https://www.ncbi.nlm.nih.gov/pubmed/27661011
https://www.ncbi.nlm.nih.gov/pubmed/27749535
https://www.ncbi.nlm.nih.gov/pubmed/27857782
https://www.ncbi.nlm.nih.gov/pubmed/27927221
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1567854
splenic cyst
http://omicsonline.org/open-access/permanent-neonatal-dm-in-monozygotic-twins-with-pcy-mutation-in-ins-gene-2155-6156.1000332.pd
http://www.ncbi.nlm.nih.gov/pubmed/24812610
Recent Publications
Down syndrome patients with normal hearts: are they really normal?
Pediatric myelin oligodendrocyte glycoprotein antibody associated disease-Asymmetric papilledema and elevated ICP are two of the chameleons: A case report.
An Unusual Case of Headache in a Child: Idiopathic Intracranial Hypertension with Diagnostic Challenge.
The Asia Pacific Pediatric Association (APPA) position statement on the MAFLD definition of fatty liver disease.
Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation.
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