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List of works by Chokri Mhiri

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

scientific article

A rare cause of myopathic syndrome: alcoholism ⬇️

scientific article published in March 1999

Acute aortic dissection presenting as painless paraplegia: a case report

scientific article published on 5 April 2016

Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia

scientific article published on 06 June 2013

Atypical onset corticobasal degeneration

scientific article published on 6 November 2015

Benign intracranial hypertension induced by doxycycline ⬇️

scientific article published on 01 May 2008

CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.

scientific article published on 12 May 2009

Carcinomatous meningitis revealing a cancer: study of two cases ⬇️

scientific article published on 01 April 2001

Cerebral rheumatoid vasculitis: a case report

scientific article

Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study

scientific article published in January 1988

Clinical features and disability progression in multiple sclerosis in Tunisia: do we really have a more aggressive disease course?

scientific article published on 2 June 2014

Clinical spectrum of cobalamin deficiency in Tunisia

scientific article published on March 2007

Cytomegalovirus (CMV) and human immunodeficiency virus (HIV) co-infection, of multinucleated giant cells in acquired immunodeficiency syndrome (AIDS) encephalopathy

scientific article published in January 1990

Cytomegalovirus (CMV) encephalomyeloradiculitis and human immunodeficiency virus (HIV) encephalitis: presence of HIV and CMV co-infected multinucleated giant cells

scientific article published in January 1990

Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy.

scientific article published on January 2013

Detection of fragile X syndrome by molecular hybridization in 29 families affected by hereditary mental retardation ⬇️

scientific article published on 01 August 1998

Duchenne muscular dystrophy: clinico-pathologic study of 10 families from South Tunisia ⬇️

scientific article published in February 1996

Focal myelin thickenings in a peripheral neuropathy associated with IgM monoclonal gammopathy

scientific article published on 01 January 1989

Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity

scientific article

Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome

scientific article

Impact of physical disability and concomitant emotional disturbances on post-stroke quality of life

scientific article published on 20 September 2016

Inclusion body myositis in French patients. A clinicopathological evaluation

scientific article published on 01 August 1990

Interleukin-1 expression in inflammatory myopathies: evidence of marked immunoreactivity in sarcoid granulomas and muscle fibres showing ischaemic and regenerative changes

scientific article published on 01 April 1997

Interleukin-1 expression in normal motor endplates and muscle fibers showing neurogenic changes

scientific article published on 01 September 1997

Iron pigment deposits, small vessel vasculitis, and erythrophagocytosis in the muscle of human immunodeficiency virus-infected patients

scientific article published in December 1991

Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia

scientific article

Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients

scientific article (publication date: 2003)

Molecular analysis of ten families with Duchenne muscular atrophy ⬇️

scientific article published on 01 March 1996

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

scientific article published on 13 December 2007

Myelopathy after zoster virus infection in immunocompetent patients: A case series

scientific article published on 23 April 2019

Necrotizing vasculitis and HIV replication in peripheral nerves

scientific article published on 01 September 1989

Paraneoplastic cerebellar degeneration as the presenting manifestation of breast carcinoma: a case report

scientific article

Paraplégie spastique familiale avec amyotrophie sévère des mains (syndrome de Silver?)

scientific article published on 01 April 2007

Peripheral neuropathy in a sporadic case of cerebrotendinous xanthomatosis

scientific article published in January 1991

Polysaccharide storage myopathy--case report and literature review.

scientific article

Primary brain lymphoma in a renal transplant patient: unsuccessful intrathecal treatment with anti-B cell monoclonal antibodies (anti-CD21)

scientific article published on 01 April 1995

Progressive multifocal leukoencephalitis complicating polymyositis

scientific article published on February 2003

Pseudo-oligodendrogliomatous meningioma. Report of 2 cases and review of the literature

scientific article published in January 1991

Relationship between muscular strength, gait and postural parameters in multiple sclerosis

scientific article published on 09 March 2011

SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum

scientific article

Sacral meningeal arteriovenous fistula supplied by branches of the hypogastric artery revealed by conus medullaris infarction

scientific article published in November 2000

Spastic paraplegia 15: linkage and clinical description of three Tunisian families

scientific article

The HIV wasting syndrome

scientific article published in July 1992

The spectrum of vasculitis in human immunodeficiency virus-infected patients. A clinicopathologic evaluation

scientific article published in August 1993

Trigeminal somatosensory evoked potentials in trichloroethylene-exposed workers

scientific article published in April 2004

Vertebral solitary bone plasmacytoma in a young adult with Trisomy 21: A case report

scientific article published on 17 December 2018

Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation

scientific article published on 25 May 2016

Zidovudine myopathy: a distinctive disorder associated with mitochondrial dysfunction

scientific article

[A novel mutation in ATP7B gene associated with severe neurological impairment in Wilson's disease]

scientific article published on 29 December 2009

[A psychiatric disorder reveals a neurobrucellosis].

scientific article published on 2 November 2016

[Cardiac involvement in Steinert myotonic dystrophy]

scientific article published on 14 March 2009

[Clinical, biological and genetic study of 24 patients with ataxia telangiectasia from southern Tunisia]

scientific article published on 01 July 2000

[Cytomegalovirus encephalo-myelo-radiculitis in acquired immunodeficiency syndrome]

scientific article published on 01 January 1990

[Hemichorea caused by striatal infarct in a young type 1 diabetic patient]

scientific article published on 01 October 2001

[Hydatid cysts of the brain stem. Two cases]

scientific article published on 01 November 1999

[Importance of electromyography in the diagnosis of botulism]

scientific article published on 01 June 1997

[Intracerebral schwannoma. Apropos of a case]

scientific article published on 01 January 1988

[Lupic spinal cord diseases and antiphospholipid antibodies]

scientific article published on 01 March 1997

[Multiple arterial thrombosis in Behçet's disease]

scientific article published on 01 April 2010

[Myasthenia gravis and hyperthyroidism: two cases]

scientific article published on 01 June 2006

[Nemaline myopathy in a patient with AIDS]

[Neurological manifestations indicative of brucellosis]

scientific article published on 01 March 1999

[Optic neuritis: Rare manifestation of neurobrucellosis]

scientific article published on 06 July 2015

[Papillary fibroelastoma of mitral leaflet revealed by a cerebrovascular accident. Case report]

scientific article published on 06 June 2008

[Relevance of plasma exchange in the treatment of myasthenia gravis: study of 11 cases]

scientific article published on 25 October 2007

[Rett's syndrome: report of 5 cases in Tunisia]

scientific article published on 01 November 1999

[Subacute myelitis revealed by human immunodeficiency virus infection]

scientific article published on 01 May 2003

[Syringomyelobulbia associated with cervical spondylosis. Pathophysiology and therapeutic implications]

scientific article published on 01 May 2002

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