Pages that link to "Q56860982"
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The following pages link to Christine Tranchant (Q56860982):
Displaying 50 items.
- Pleiotropic effects of the 8.1 HLA haplotype in patients with autoimmune myasthenia gravis and thymus hyperplasia (Q24562160) (← links)
- ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency (Q24656191) (← links)
- Effectiveness of anti-psychotics and related drugs in the Huntington French-speaking group cohort (Q28538703) (← links)
- Blood Cell Palmitoleate-Palmitate Ratio Is an Independent Prognostic Factor for Amyotrophic Lateral Sclerosis (Q28546154) (← links)
- Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy (Q29147504) (← links)
- The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation (Q30570939) (← links)
- [Autoimmune encephalitis, clinical, radiological and immunological data]. (Q30574740) (← links)
- ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations. (Q30688374) (← links)
- Neuroendocrine disturbances in Huntington's disease (Q33421708) (← links)
- [Autosomal recessive cerebellar ataxias]. (Q33445775) (← links)
- Peripheral neuropathies associated with hereditary cerebellar ataxias (Q33783057) (← links)
- Immediate effects of 14 non MAOI antidepressants in rats with spontaneous petit mal-like seizures (Q34149040) (← links)
- Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders (Q34170998) (← links)
- Next generation sequencing for molecular diagnosis of neuromuscular diseases. (Q34242488) (← links)
- The autosomal recessive cerebellar ataxias (Q34254468) (← links)
- Methylphenidate for gait hypokinesia and freezing in patients with Parkinson's disease undergoing subthalamic stimulation: a multicentre, parallel, randomised, placebo-controlled trial (Q34278569) (← links)
- Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. (Q34295566) (← links)
- Association between caffeine intake and age at onset in Huntington's disease (Q34348412) (← links)
- Acute myelitis and Lyme disease (Q34717377) (← links)
- Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study (Q35061314) (← links)
- SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia (Q35125192) (← links)
- COMT Val158Met Polymorphism Modulates Huntington's Disease Progression (Q36140827) (← links)
- Normalisation of brain spectroscopy findings in Niemann-Pick disease type C patients treated with miglustat (Q36879362) (← links)
- Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression (Q37350136) (← links)
- Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy (Q37408211) (← links)
- Pathophysiogical and therapeutic progress in Friedreich ataxia (Q38208992) (← links)
- Dehydroepiandrosterone for myotonic dystrophy type 1. (Q38388268) (← links)
- Movement disorders in mitochondrial diseases. (Q38914023) (← links)
- New insights into orthostatic hypotension in multiple system atrophy: a European multicentre cohort study. (Q39006423) (← links)
- Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects (Q39412774) (← links)
- Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias (Q39486694) (← links)
- Validation of a clinical practice-based algorithm for the diagnosis of autosomal recessive cerebellar ataxias based on NGS identified cases (Q39797467) (← links)
- Early onset collagen VI myopathies: Genetic and clinical correlations (Q39823975) (← links)
- Low cancer prevalence in polyglutamine expansion diseases (Q40334409) (← links)
- Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease (Q41168222) (← links)
- Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2). (Q42236757) (← links)
- Familial motor neuron disease with Lewy body-like inclusions in the substantia nigra, the subthalamic nucleus, and the globus pallidus (Q42451509) (← links)
- Muscular mitochondrial function in amyotrophic lateral sclerosis is progressively altered as the disease develops: A temporal study in man (Q42483253) (← links)
- Platelet functions, alpha 2-adrenergic receptors and cytoplasmic free calcium are normal in the myotonic dystrophy of Steinert. (Q42510101) (← links)
- Mitochondrial respiratory chain function in skeletal muscle of ALS patients. (Q42527324) (← links)
- The neurophysiological features of myoclonus-dystonia and differentiation from other dystonias (Q42648922) (← links)
- Quality of life in Parkinson's disease improved by apomorphine pump: the OPTIPUMP cohort study (Q42688217) (← links)
- Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation. (Q42735789) (← links)
- Inaugural audiovisual impairment disclosing specific neurological disorders (Q42788471) (← links)
- Myopathies in the elderly: a hospital-based study. (Q42973670) (← links)
- Symptomatic paroxysmal dysarthria-ataxia in demyelinating diseases (Q43115295) (← links)
- Neuromuscular symptoms and elevated creatine kinase after statin withdrawal. (Q43165963) (← links)
- Muscle phosphorylase b kinase deficiency revisited. (Q43192011) (← links)
- Doxycycline in Creutzfeldt-Jakob disease: a phase 2, randomised, double-blind, placebo-controlled trial. (Q43497178) (← links)
- Encelopathies caused by prions (Q44361218) (← links)