Ichraf Kraoua - Neurology

Author Information

Ichraf Kraoua is a distinguished researcher affiliated with the Child Neurology, Department of Child and Adolescent Neurology at the National Institute Mongi Ben Hmida of Neurology in Tunis, Tunisia. Her work primarily focuses on neurological disorders in children and adolescents, with a significant emphasis on genetic and clinical features of rare syndromes and conditions. Her research is conducted in collaboration with the UR 12SP24 at the same institute, highlighting her commitment to advancing the understanding of pediatric neurology.

Research Contributions

Dr. Ichraf Kraoua has made substantial contributions to the field of child neurology, particularly in understanding Cockayne syndrome and other rare neurogenetic disorders. Her work has explored the clinical variability and genetic underpinnings of conditions such as Cockayne syndrome, autoimmune encephalitis, and hypomyelinating leukodystrophies. She has also investigated the epidemiological and clinical characteristics of neurodegeneration with brain iron accumulation in children. Her research is pivotal in elucidating the genetic and clinical complexities of these disorders, thereby informing better diagnostic and therapeutic strategies.

Aliases

Dr. Ichraf Kraoua is also known by the aliases I Kraoua and I. Kraoua in academic publications. These variations are used interchangeably in different research articles and databases.

Publication and Citation Metrics

Metric	Value
Publication Count	94
Citation Count	482
h-index	10

Publications:

Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations

DOI: 10.1186/s13023-022-02257-1

Year: 2022

Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B

DOI: 10.3390/genes12121922

Year: 2021

Heterogeneous clinical features in Cockayne syndrome-A patients with the same mutation and in siblings

DOI: 10.21203/RS.3.RS-603999/V1

Year: 2021

Conversion disorder in children and adolescents : Clinical features of pseudoneurological symptoms

DOI: 10.1192/j.eurpsy.2021.490

Year: 2021

Acute Movement Disorders in Childhood

DOI: 10.1097/PEC.0000000000002017

Year: 2021

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

DOI: 10.1371/journal.pone.0258202

Year: 2021

Epidemiological, clinical and paraclinical characteristics of neurodegeneration with brain iron accumulation in childhood

DOI: 10.1016/j.jns.2021.118884

Year: 2021

Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort

DOI: 10.1155/2021/6666117

Year: 2021

Genetic characterization of hypomyelinating leukodystrophies in the Tunisian cohort

DOI: 10.1016/j.jns.2021.118263

Year: 2021

Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.

DOI: 10.1055/s-0041-1728654

Year: 2021

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