Dr Jehan Suleiman, MD FRACP PhD - University of Sydney

Dr Jehan Suleiman

MD FRACP PhD

University of Sydney

Australia

Main Specialties: Pediatrics

Additional Specialties: Pediatrics, Paediatric Neurology

ORCID logohttps://orcid.org/0000-0003-0914-7650

Dr Jehan Suleiman, MD FRACP PhD - University of Sydney

Dr Jehan Suleiman

MD FRACP PhD

Introduction

Primary Affiliation: University of Sydney - Australia

Specialties:

Additional Specialties:

Research Interests:

Education

Jan 2013
University of Sydney
PhD
Medicine
Jan 2012
Royal Australasian College of Physicians
FRACP
PAediatrics

Experience

Jan 2013
Children's Hospital at Westmead

Neurology
Jan 2013
Children's Hospital at Westmead

Neurology
Jan 2013
Children's Hospital at Westmead

Neurology
Jan 2013
Children's Hospital at Westmead

Neurology
Jan 2013
Children's Hospital at Westmead

Neurology
Jan 2013
Children's Hospital at Westmead

Neurology
Jan 2013
Children's Hospital at Westmead

Neurology
Jan 2013
Children's Hospital at Westmead

Neurology
Feb 2009
Children Hospital at westmead

Neurology
University of Sydney

Sydney Medical School, Paediatrics & Child Health
United Arab Emirates University

Pediatrics
Al Tawam Hospital
Consultant Pediatric Neurologist
Pediatric

Publications

36Publications

612Reads

1661Profile Views

48PubMed Central Citations

Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases.

Mol Genet Metab 2018 Dec 16;125(4):315-321. Epub 2018 Oct 16.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Texas Children's Hospital, Houston, TX, USA; Joint BCM-CUHK Center of Medical Genetics, Prince of Wales Hospital, ShaTin, Hong Kong Special Administrative Region. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2018.10.003DOI Listing
December 2018
2 Reads
2.625 Impact Factor

West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutations.

Epileptic Disord 2018 Oct;20(5):401-412

Division of Neurology, Department of Pediatrics, Tawam Hospital, Al Ain, Department of Pediatrics, College of Medicine and Health Sciences UAE University, Al Ain, United Arab Emirates.

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http://dx.doi.org/10.1684/epd.2018.1005DOI Listing
October 2018
82 Reads
0.900 Impact Factor

ATP13A2 novel mutations causing a rare form of juvenile-onset Parkinson disease.

Brain Dev 2018 Oct 11;40(9):824-826. Epub 2018 Jun 11.

Division of Clinical Genetics and Metabolic Disorders, Tawam Hospital, Al Ain, United Arab Emirates. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2018.05.017DOI Listing
October 2018
17 Reads
1.542 Impact Factor

PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities.

Clin Genet 2018 Oct 25;94(3-4):351-355. Epub 2018 Jun 25.

Division of Genetic and Metabolic Disorders, Pediatrics Department, Tawam Hospital, Al Ain, United Arab Emirates.

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http://doi.wiley.com/10.1111/cge.13387
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http://dx.doi.org/10.1111/cge.13387DOI Listing
October 2018
79 Reads
3.931 Impact Factor

B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss.

Neuropediatrics 2018 Aug 23;49(4):289-295. Epub 2018 May 23.

Division of Neurology, Department of Pediatric, Tawam Hospital, Al Ain, United Arab Emirates.

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http://www.thieme-connect.de/DOI/DOI?10.1055/s-0038-1651519
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http://dx.doi.org/10.1055/s-0038-1651519DOI Listing
August 2018
92 Reads
1.104 Impact Factor

Pediatric Multiple Sclerosis in the United Arab Emirates: Characteristics From a Multicenter Study and Global Comparison.

J Child Neurol 2018 May 1;33(6):422-427. Epub 2018 Apr 1.

8 Department of Neurology, Johns Hopkins University, Baltimore, MD, USA.

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http://dx.doi.org/10.1177/0883073818759103DOI Listing
May 2018
32 Reads
1.670 Impact Factor

Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus.

BMC Med Genet 2018 03 2;19(1):34. Epub 2018 Mar 2.

Department of Paediatrics, College of Medicine and Heath Sciences, United Arab Emirates University, P.O. Box 17666, Al-Ain, United Arab Emirates.

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https://bmcmedgenet.biomedcentral.com/articles/10.1186/s1288
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http://dx.doi.org/10.1186/s12881-018-0540-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834892PMC
March 2018
28 Reads
1 Citation
2.083 Impact Factor

WDR45B-related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome.

Clin Genet 2018 Feb 7;93(2):360-364. Epub 2017 Sep 7.

Division of Genetic and Metabolic Disorders, Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates.

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http://dx.doi.org/10.1111/cge.13054DOI Listing
February 2018
44 Reads
3.931 Impact Factor

17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report.

BMC Med Genet 2017 10 25;18(1):119. Epub 2017 Oct 25.

Division of Clinical Genetics and Metabolic Disorders, Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates.

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http://dx.doi.org/10.1186/s12881-017-0479-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5657100PMC
October 2017
35 Reads
2.083 Impact Factor

A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataract.

Meta Gene 2016 Sep 18;9:124-7. Epub 2016 May 18.

Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.

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http://dx.doi.org/10.1016/j.mgene.2016.05.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908276PMC
September 2016
27 Reads
2 Citations

Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family.

Am J Med Genet A 2016 Feb 5;170A(2):540-543. Epub 2015 Oct 5.

Department of Pediatrics, College of Medicine and Heath Sciences, United Arab Emirates University, United Arab Emirates.

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http://doi.wiley.com/10.1002/ajmg.a.37421
Publisher Site
http://dx.doi.org/10.1002/ajmg.a.37421DOI Listing
February 2016
30 Reads
1 Citation
2.160 Impact Factor

The recognition and treatment of autoimmune epilepsy in children.

Dev Med Child Neurol 2015 May 8;57(5):431-40. Epub 2014 Dec 8.

Department of Paediatrics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates; Paediatrics and Child Health Discipline, Clinical School, The Children's Hospital at Westmead, Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

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http://dx.doi.org/10.1111/dmcn.12647DOI Listing
May 2015
34 Reads
2 Citations
3.510 Impact Factor

Autoantibodies to neuronal antigens in children with new-onset seizures classified according to the revised ILAE organization of seizures and epilepsies.

Epilepsia 2013 Dec 23;54(12):2091-100. Epub 2013 Oct 23.

Neuroimmunology Group, Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, University of Sydney, Sydney, New South Wales, Australia; T.Y. Nelson Department of Neurology, Children's Hospital at Westmead, University of Sydney, Sydney, New South Wales, Australia.

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http://dx.doi.org/10.1111/epi.12405DOI Listing
December 2013
29 Reads
12 Citations
4.571 Impact Factor

Autoimmune epilepsy in children: case series and proposed guidelines for identification.

Epilepsia 2013 Jun 28;54(6):1036-45. Epub 2013 Mar 28.

Neuroimmunology Group, Institute for Neuroscience and Muscle Research, the Children's Hospital at Westmead, University of Sydney, Sydney, New South Wales, Australia.

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http://dx.doi.org/10.1111/epi.12142DOI Listing
June 2013
41 Reads
10 Citations
4.571 Impact Factor

Immune-mediated steroid-responsive epileptic spasms and epileptic encephalopathy associated with VGKC-complex antibodies.

Dev Med Child Neurol 2011 Nov 30;53(11):1058-60. Epub 2011 Aug 30.

Neuroimmunology Group, Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, University of Sydney, Sydney, New South Wales, Australia.

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http://dx.doi.org/10.1111/j.1469-8749.2011.04096.xDOI Listing
November 2011
17 Reads
6 Citations
3.510 Impact Factor

Severe encephalopathy with swine origin influenza A H1N1 infection in childhood: case reports.

Neurology 2010 Mar 3;74(13):1077-8. Epub 2010 Mar 3.

Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead NSW 2145, Australia.

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http://dx.doi.org/10.1212/WNL.0b013e3181d6b113DOI Listing
March 2010
2 Reads
12 Citations
8.290 Impact Factor

Top co-authors

Russell C Dale
Russell C Dale

University of Sydney

4
Bassam R Ali
Bassam R Ali

United Arab Emirates University

4
Angela Vincent
Angela Vincent

John Radcliffe Hospital

3
Lihadh Al-Gazali
Lihadh Al-Gazali

United Arab Emirates University

3
Bethan Lang
Bethan Lang

University of Oxford

3
Fabienne Brilot
Fabienne Brilot

University of Sydney

3
Deepak Gill
Deepak Gill

University of Sydney

2
Anne John
Anne John

United Arab Emirates University

2