Concepedia

Author

Dina Ramadan

Al-Sabah Hospital

Also Known As

Ahmed Nafea, D G Ramadan, D. G. Ramadan, D.G. Ramadan, Dina G Ramadan, Dina G. Ramadan, Dina Ramadan

32

Publications

905

Citations

14

H-Index

37

Concepts

All Affiliations

Al-Sabah HospitalKuwait UniversityFarwaniya HospitalUniversity College LondonAdan Hospital
DR

About

Dina Ramadan is an author at Al-Sabah Hospital specializing in medicine, pathology, and autoimmunity.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

8

8

668

2

Gastroenterology

2

2

477

3

Health Sciences

1

1

35

4

Biochemistry

1

1

20

5

Cell Biology

1

1

56

Dina Ramadan

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14

Publications

836

Citations

13

H-Index

YearCitations

Loss of Interleukin-10 Signaling and Infantile Inflammatory Bowel Disease: Implications for Diagnosis and Therapy

Daniel Kotlarz, Rita Beier, Dhaarini Murugan,

Gastroenterology

2012

462

Differentiating the roles of STAT5B and STAT5A in human CD4+ T cells

Jennifer A. Jenks, Scott M. Seki, Takahiro Kanai,

Clinical Immunology

2013

56

Costello syndrome and hyperinsulinemic hypoglycemia

Saji Alexander, Dina Ramadan, Haya Alkhayyat,

American Journal of Medical Genetics Part A

2005

42

Acute pyelonephritis and renal scarring in Kuwaiti children: a follow-up study using 99mTc DMSA renal scintigraphy

Mohamed Zaki, Mona Badawi, Ghalia Al Mutari,

Pediatric Nephrology

2005

39

Liver Disease and Other Comorbidities in Wolcott-Rallison Syndrome: Different Phenotype and Variable Associations in a Large Cohort

Abdelhadi Habeb, Asma Deeb, Matthew B. Johnson,

Hormone Research in Paediatrics

2015

39

Whole-exome sequencing gives additional benefits compared to candidate gene sequencing in the molecular diagnosis of children with growth hormone or IGF-1 insensitivity

L Shapiro, Sumana Chatterjee, Dina Ramadan,

European Journal of Endocrinology

2017

38

Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster.

Mohamed Sabry, Maha S. Zaki, Shabbeer Hassan,

Journal of Medical Genetics

1998

35

Infantile Hyperinsulinism Associated with Enteropathy, Deafness and Renal Tubulopathy: Clinical Manifestations of a Syndrome Caused by a Contiguous Gene Deletion Located on Chromosome 11p

Khalid Hussain, Maria Bitner‐Glindzicz, Diana C. Blaydon,

Journal of Pediatric Endocrinology and Metabolism

2004

23

Lactic acidosis and developmental delay due to deficiency of E3 binding protein (protein X) of the pyruvate dehydrogenase complex

Dina Ramadan, R. A. Head, Asmaa Al-Tawari,

Journal of Inherited Metabolic Disease

2004

21

An early onset form of methylenetetrahydrofolate reductase deficiency: a report of a family from Kuwait

Asma Abdullah Al Tawari, Dina Ramadan, David Neubauer,

Brain and Development

2002

20

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