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A. Boukhris
Affiliation : Hopital Universitaire Habib Bourguiba
- 27Publications (affiliation in Tunisia)
- 38Total publications
- 1556Citations
- 13h-index
Research profile
A. Boukhris has 27 indexed publications (2007–2017). Their work appears mainly in “Revue Neurologique”, “Journal of the Neurological Sciences” and “The American Journal of Human Genetics”. Their most cited article, “Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuro” (2007), has been cited 257 times. Their work is co-authored with at least 12 researchers, including institutions in France, Italy, Argentina.
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Create my free profile Add my publicationsResearch areas
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Genetic and Kidney Cyst Diseases
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
Publications (27)
- Features of hereditary spastic paraplegias in North African region
- Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia
- Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia
- Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy
- Selective bilateral thalamic necrosis following carbon monoxide poisoning: Case report
- Les caractéristiques cliniques et étiologiques des chorées dans le sud Tunisien
- Characteristics of motor complications in patients with Parkinson's/INS; disease in southern Tunisia (ST)
- Atypical neurological presentation of GSS: Case report
- Characteristics of Parkinson's disease dementia in Southern Tunisia
- Étude de corrélation clinique et radiologique dans la sclérose en plaques : à propos de 182 cas
- La maladie de Wilson avec atteintes neurologiques dans le sud tunisien : étude clinique et génétique de 12 cas
- Combination of Positional Cloning and New Generation Sequencing Identifies 3 Novel Genes in Spastic Paraplegia Involved in Common Metabolic Pathways (P01.205)
- REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction
- Depression, anxiety and multiple sclerosis: Links with alexithymia
- A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum
- Dépression, coping et qualité de vie dans la maladie de Parkinson. À propos de 50 patients tunisiens
- Dépression, coping et qualité de vie dans la maladie de Parkinson. À propos de 50 patients tunisiens
- CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5
- Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity
- Nouvelle mutation du gène ATP7B responsable d’une maladie de Wilson avec atteinte neurologique sévère
- Paraplégie spastique avec atteinte mentale et atrophie du corps calleux
- Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome
- Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration
- Spastic paraplegia 15: Linkage and clinical description of three Tunisian families
- Paraplégie spastique familiale avec amyotrophie sévère des mains (syndrome de Silver?)
- E - 3 Les paraplégies spasmodiques familiales : à propos de 33 familles du sud tunisien
- L - 11 Tuberculome intradural extramédullaire compliquant une méningo-encéphalo-radiculite tuberculeuse : à propos d’un cas
Publication venues
- Revue Neurologique × 7
- Journal of the Neurological Sciences × 5
- The American Journal of Human Genetics × 3
- L information psychiatrique × 2
- Brain × 2
- Annals of Indian Academy of Neurology × 1
Publications per year
- 20171
- 20138
- 20123
- 20112
- 20103
- 20094
- 20081
- 20075
Collaborations
Partner institutions : Inserm · Université Pierre-et-Marie-Curie · Pitié-Salpêtrière Hospital · Bambino Gesù Children's Hospital · Hebrew University of Jerusalem
Co-authors’ countries : France · Italy · Argentina
Co-authors
- Chokri Mhiri
- Imed Feki
- M. Imed Miladi
- Nizar Elleuch
- Mariem Damak
- Imen Bouchhima
- Elyes Turki
- Mohamed Imed Miladi
- Chahira Hachicha
- Othman Amami
- Salma Smaoui
- C. Triki
Bibliographic data from OpenAlex (open database).
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