Author

Essam A. R. Ismail

Observed names: Essam A Ismail, Essam A. Ismail, Essam A.R. Ismail, Essam Ar Ismail

Institution: Farwaniya Hospital

Observed institutions: Metropolitan Hospital Center, Farwaniya Hospital, Kuwait University, The Ohio State University, Hacettepe University

OpenAlex ID: A5103390360

Congenital Insensitivity to Pain with Anhidrosis: Novel Mutations in the TRKA (NTRK1) Gene Encoding A High-Affinity Receptor for Nerve Growth Factor

1999 · Sek Mardy, Yuichi Miura, et al. · The American Journal of Human Genetics · 156

Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene

2005 · Stephan M. Tanner, Zhongyuan Li, et al. · Proceedings of the National Academy of Sciences · 110

Genetically heterogeneous selective intestinal malabsorption of vitamin B12: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East

2004 · Stephan M. Tanner, Zhongyuan Li, et al. · Human Mutation · 94

Congenital insensitivity to pain with anhidrosis (CIPA): Novel mutations of theTRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutantTRKA andPKLR genes in a family with CIPA and pyruvate kinase deficiency

2001 · Yasuhiro Indo, Sek Mardy, et al. · Human Mutation · 66

Neonatal suppurative parotitis over the last 4 decades: Report of three new cases and review

2012 · Essam A Ismail, Tarek M Seoudi, et al. · Pediatrics International · 61

A Fatal Small Dose of Phosphate Enema in a Young Child With No Renal or Gastrointestinal Abnormality

2000 · Essam A. R. Ismail, Ghalia Al‐Mutairi, et al. · Journal of Pediatric Gastroenterology and Nutrition · 41

Congenital Insensitivity to Pain With Anhidrosis: Lack of Eccrine Sweat Gland Innervation Confirmed

1998 · Essam A. R. Ismail, Nufood Al-Shammari, et al. · Journal of Child Neurology · 35

An Epidemiologic, Clinical, and Therapeutic Study of Childhood Guillain-Barré Syndrome in Kuwait: Is It Related to the Oral Polio Vaccine?

1998 · Essam A. R. Ismail, Issa S. Shabani, et al. · Journal of Child Neurology · 24

Allgrove syndrome with features of familial dysautonomia: A novel mutation in the AAAS gene

2006 · Essam A. Ismail, Anna Tulliot‐Pelet, et al. · Acta Paediatrica · 19

Congenital absence of the infrahepatic segment of the inferior vena cava with deep venous thrombosis in an 8.5‐year‐old boy

2010 · Essam A. Ismail, Asmaa F. Azab, et al. · Pediatrics International · 10

Persistent hyperinsulinaemic hypoglycaemia of infancy (nesidioblastosis): a report from Kuwait

1999 · Dina G. Ramadan, Mona H. Badawi, et al. · Annals of Tropical Paediatrics · 8

Ethylmalonic encephalopathy. Another patient from Kuwait

2009 · Essam A. Ismail, Tarek M. Seoudi, et al. · Neurosciences · 4

Chronic infantile neurological cutaneous articular syndrome in an Arab patient

2001 · Essam Ar Ismail, Michael J Dillon, et al. · Pediatrics International · 1

Transient hypocalcemia with elevated serum parathormone in an infant of a hyperparathyroid mother

1998 · Essam A.R. Ismail, Nufood Al‐Shammari, et al. · Pediatrics International · 1

Intestinal Malrotation in Children beyond the Neonatal Period: Report of Two Cases with Rare Presentations

2008 · Dina G. Ramadan, Mohamed Zaki, et al. · Medical Principles and Practice

Incomplete form of chronic infantile neurological cutaneous and articular syndrome

2000 · Essam Ar Ismail · Pediatrics International

Works count: 16

Citation count: 630

H-index: 10

I10-index: 10