Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Sabrina Debruxelles »
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Sabrina Boulet < Sabrina Debruxelles < Sabrina Wagner  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 2.
Ident.Authors (with country if any)Title
000262 (2009) Fabienne Ory-Magne [France] ; Christine Brefel-Courbon [France] ; Pierre Payoux [France] ; Sabrina Debruxelles [France] ; Igor Sibon [France] ; Cyril Goizet [France] ; Pierre Labauge [France] ; Patrice Menegon [France] ; Emmanuelle Uro-Coste [France] ; Bernardino Ghetti [États-Unis] ; Marie Bernadetle Delisle [France] ; Ruben Vidal [États-Unis] ; Olivier Rascol [France]Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498‐499InsTC)
000270 (2009) Fabienne Ory-Magne [France] ; Christine Brefel-Courbon [France] ; Pierre Payoux [France] ; Sabrina Debruxelles [France] ; Igor Sibon [France] ; Cyril Goizet [France] ; Pierre Labauge [France] ; Patrice Menegon [France] ; Emmanuelle Uro-Coste [France] ; Bernardino Ghetti [États-Unis] ; Marie Bernadetle Delisle [France] ; Ruben Vidal [États-Unis] ; Olivier Rascol [France]Clinical Phenotype and Neuroimaging Findings in a French Family with Hereditary Ferritinopathy (FTL498-499InsTC)

List of associated KwdEn.i

Nombre de
documents
Descripteur
2Phenotype
1Adult
1Age of Onset
1Apoferritins (genetics)
1Basal Ganglia Diseases (genetics)
1Basal Ganglia Diseases (metabolism)
1Basal Ganglia Diseases (pathology)
1Basal Ganglia Diseases (radionuclide imaging)
1Basal ganglion
1Central Nervous System (chemistry)
1Central Nervous System (pathology)
1Cerebellar Ataxia (genetics)
1Cerebellar Ataxia (metabolism)
1Cerebellar Ataxia (pathology)
1Cerebellar Ataxia (radionuclide imaging)
1Dementia (genetics)
1Dementia (metabolism)
1Dementia (pathology)
1Dementia (radionuclide imaging)
1Female
1Ferritin
1Ferritins (analysis)
1France (epidemiology)
1French
1Humans
1Iron
1Iron (analysis)
1Liver (chemistry)
1Liver (pathology)
1Magnetic Resonance Imaging
1Male
1Middle Aged
1Movement Disorders (genetics)
1Movement Disorders (metabolism)
1Movement Disorders (pathology)
1Movement Disorders (radionuclide imaging)
1Muscle, Skeletal (chemistry)
1Muscle, Skeletal (pathology)
1Mutagenesis, Insertional
1Mutation
1Nervous system diseases
1Pedigree
1Positron-Emission Tomography
1Skin (chemistry)
1Skin (pathology)
1Tremor (genetics)
1Tremor (metabolism)
1Tremor (pathology)
1Tremor (radionuclide imaging)
1basal ganglia
1ferritin
1hereditary ferritinopathy
1iron
1neuroferritinopathy

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