List of works - Jehan Suleiman

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.

scientific article published on 25 October 2017

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

scientific article published on 18 May 2016

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

scientific article published on 11 June 2018

ATP13A2-related juvenile-onset Parkinson disease

scientific article published on 23 August 2018

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

scientific article published on 23 October 2013

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.

scientific article

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

scientific article published on 5 October 2015

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

scientific article

Correction to: Expanding the genetic heterogeneity of intellectual disability.

scientific article published on 29 December 2017

Expanding the genetic heterogeneity of intellectual disability

scientific article published on 22 September 2017

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

scientific article published on August 30, 2011

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

scientific article published on 16 October 2018

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

scientific article published on 25 June 2018

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

scientific article published on 01 April 2018

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

scientific article published on 3 March 2010

TASP1 is deleted in an infant with developmental delay, microcephaly, distinctive facial features, and multiple congenital anomalies.

scientific article published on 6 April 2018

VGKC antibodies in pediatric encephalitis presenting with status epilepticus.

scientific article

VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features

scientific article published on 26 December 2019

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

scientific article

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

scientific article published on 01 October 2018

List of works by Jehan Suleiman

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.

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

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

ATP13A2-related juvenile-onset Parkinson disease

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

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.

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

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

Correction to: Expanding the genetic heterogeneity of intellectual disability.

Expanding the genetic heterogeneity of intellectual disability

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

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

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

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

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

TASP1 is deleted in an infant with developmental delay, microcephaly, distinctive facial features, and multiple congenital anomalies.

VGKC antibodies in pediatric encephalitis presenting with status epilepticus.

VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features

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

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