Naglaa M Kamal
Professor of Pediatrics and Pediatric Hepatology, Pediatric Hepatology Unit, Faculty of Medicine, Cairo University
(email)
Pages that link to Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study.
View
What links here
No backlinks found.
Publications
Bio
Classes
Links
Calendar
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
