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Articles in journal or book chapters
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A. Le Floch,
M. Vidailhet,
C. Flamand-Rouviere,
D. Grabli,
J. M. Mayer,
M. Gonce,
E. Broussolle,
and E. Roze.
Table tennis dystonia.
Mov Disord,
2010.
Note: Journal articleofficial journal of the Movement Disorder Society.
[WWW]
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S. Leu-Semenescu,
I. Arnulf,
C. Decaix,
F. Moussa,
F. Clot,
C. Boniol,
Y. Touitou,
R. Levy,
M. Vidailhet,
and E. Roze.
Sleep and rhythm consequences of a genetically induced loss of serotonin.
Sleep,
33(3):307-14,
2010.
Note: Journal ArticleUnited States.
[WWW]
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F. Clot,
D. Grabli,
C. Cazeneuve,
E. Roze,
P. Castelnau,
B. Chabrol,
P. Landrieu,
K. Nguyen,
G. Ponsot,
M. Abada,
D. Doummar,
P. Damier,
R. Gil,
S. Thobois,
A. J. Ward,
M. Hutchinson,
A. Toutain,
F. Picard,
A. Camuzat,
E. Fedirko,
C. San,
D. Bouteiller,
E. LeGuern,
A. Durr,
M. Vidailhet,
and A. Brice.
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.
Brain,
132(Pt 7):1753-63,
2009.
Note: French Dystonia NetworkJournal ArticleResearch Support, Non-U.S. Gov'tEnglanda journal of neurology.
[WWW]
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V. Cochen De Cock,
M. Abouda,
S. Leu,
D. Oudiette,
E. Roze,
M. Vidailhet,
T. Similowski,
and I. Arnulf.
Is obstructive sleep apnea a problem in Parkinson's disease?.
Sleep Med,
2009.
Note: Journal article.
[WWW]
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E. Guettard,
E. Roze,
G. Abada,
C. Lemesle,
M. Vidailhet,
A. Laurent-Vannier,
and M. P. Chevignard.
Management of spasticity and dystonia in children with acquired brain injury with rehabilitation and botulinum toxin A.
Dev Neurorehabil,
12(3):128-38,
2009.
Note: Clinical TrialJournal ArticleResearch Support, Non-U.S. Gov'tEngland.
[WWW]
Keyword(s): Activities of Daily Living,
Adolescent,
Botulinum Toxin Type A/administration & dosage/*therapeutic use,
Brain Injuries/*complications/drug therapy/rehabilitation,
Child,
Child,
Preschool,
Dystonia/*drug therapy/etiology/*rehabilitation,
Female,
Follow-Up Studies,
Gait/drug effects,
Humans,
Male,
Muscle Spasticity/*drug therapy/etiology/*rehabilitation,
*Occupational Therapy,
Pain/etiology/therapy,
Pain Measurement/methods,
*Physical Therapy Modalities,
Prospective Studies,
Recovery of Function/drug effects,
Treatment Outcome,
Young Adult.
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K. Kinugawa,
M. Vidailhet,
F. Clot,
E. Apartis,
D. Grabli,
and E. Roze.
Myoclonus-dystonia: an update.
Mov Disord,
24(4):479-89,
2009.
Note: Journal ArticleReviewUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): Diagnosis,
Differential,
Dystonia/*complications/diagnosis/genetics/therapy,
Humans,
Magnetic Resonance Imaging/methods,
Movement Disorders/genetics/*physiopathology/therapy,
Mutation/genetics,
Myoclonus/*complications/diagnosis/genetics/therapy,
Sarcoglycans/genetics.
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E. Roze,
P. Bounolleau,
D. Ducreux,
V. Cochen,
S. Leu-Semenescu,
Y. Beaugendre,
M. C. Lavallard-Rousseau,
A. Blancher,
F. Bourdain,
P. Dupont,
L. Carluer,
L. Verdure,
M. Vidailhet,
and E. Apartis.
Propriospinal myoclonus revisited: Clinical, neurophysiologic, and neuroradiologic findings.
Neurology,
72(15):1301-9,
2009.
Note: Journal ArticleUnited States.
[WWW]
Keyword(s): Adolescent,
Adult,
Aged,
Diffusion Magnetic Resonance Imaging,
Electrodiagnosis,
Electroencephalography,
Electromyography,
Evoked Potentials,
Somatosensory/physiology,
Female,
Hematologic Tests,
Humans,
Magnetic Resonance Imaging,
Male,
Middle Aged,
Myoclonus/*diagnosis/pathology/*therapy,
Neural Pathways/physiopathology,
Prospective Studies,
Spinal Cord/pathology/physiopathology,
Tomography,
X-Ray Computed,
Young Adult.
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E. Roze,
A. Soumare,
I. Pironneau,
S. Sangla,
V. C. de Cock,
A. Teixeira,
A. Astorquiza,
C. Bonnet,
J. P. Bleton,
M. Vidailhet,
and A. Elbaz.
Case-control study of writer's cramp.
Brain,
132(Pt 3):756-64,
2009.
Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglanda journal of neurology.
[WWW]
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M. Vidailhet,
D. Grabli,
and E. Roze.
Pathophysiology of dystonia.
Curr Opin Neurol,
22(4):406-413,
2009.
Note: Journal article.
[WWW]
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E. Apartis,
B. Gaymard,
S. Verhaeghe,
E. Roze,
M. Vidailhet,
and A. Lannuzel.
Predominant cortical dysfunction in Guadeloupean parkinsonism.
Brain,
131(Pt 10):2701-9,
2008.
Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglanda journal of neurology.
[WWW]
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C. Ewenczyk,
A. Leroux,
A. Roubergue,
V. Laugel,
A. Afenjar,
J. M. Saudubray,
P. Beauvais,
T. Billette de Villemeur,
M. Vidailhet,
and E. Roze.
Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum.
Brain,
131(Pt 3):760-1,
2008.
Note: Journal ArticleEnglanda journal of neurology.
[WWW]
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C. Gitiaux,
E. Roze,
K. Kinugawa,
C. Flamand-Rouviere,
N. Boddaert,
E. Apartis,
V. Valayannopoulos,
G. Touati,
J. Motte,
D. Devos,
K. Mention,
D. Dobbelaere,
D. Rodriguez,
A. Roubertie,
B. Chabrol,
F. Feillet,
M. Vidailhet,
and N. Bahi-Buisson.
Spectrum of movement disorders associated with glutaric aciduria type 1: A study of 16 patients.
Mov Disord,
2008.
Note: Journal articleofficial journal of the Movement Disorder Society.
[WWW]
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E. Guettard,
M. F. Portnoi,
K. Lohmann-Hedrich,
B. Keren,
S. Rossignol,
S. Winkler,
I. El Kamel,
S. Leu,
E. Apartis,
M. Vidailhet,
C. Klein,
and E. Roze.
Myoclonus-dystonia due to maternal uniparental disomy.
Arch Neurol,
65(10):1380-5,
2008.
Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States.
[WWW]
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D. Maltete,
P. Verdure,
E. Roze,
M. Vidailhet,
E. Apartis,
F. Bellow,
and L. Verdure.
TENS for the treatment of propriospinal myoclonus.
Mov Disord,
2008.
Note: Journal articleofficial journal of the Movement Disorder Society.
[WWW]
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E. Roze,
E. Apartis,
F. Clot,
N. Dorison,
S. Thobois,
L. Guyant-Marechal,
C. Tranchant,
P. Damier,
D. Doummar,
N. Bahi-Buisson,
N. Andre-Obadia,
D. Maltete,
A. Echaniz-Laguna,
Y. Pereon,
Y. Beaugendre,
S. Dupont,
T. De Greslan,
C. P. Jedynak,
G. Ponsot,
J. C. Dussaule,
A. Brice,
A. Durr,
and M. Vidailhet.
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations.
Neurology,
70(13):1010-6,
2008.
Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States.
[WWW]
Keyword(s): Adolescent,
Adult,
Aged,
Brain/metabolism/physiopathology,
Child,
Child,
Preschool,
DNA Mutational Analysis,
Disease Progression,
Dystonia/*diagnosis/*genetics/physiopathology,
Electroencephalography,
Female,
Genetic Markers/genetics,
Genetic Predisposition to Disease/*genetics,
Genetic Screening,
Genotype,
Humans,
Male,
Middle Aged,
Muscle,
Skeletal/metabolism/physiopathology,
Mutation/genetics,
Myoclonus/*diagnosis/*genetics/physiopathology,
Prospective Studies,
Reflex,
Abnormal/genetics,
Remission,
Spontaneous,
Sarcoglycans/*genetics.
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E. Roze,
E. Apartis,
and J. M. Trocello.
Cortical excitability in DYT-11 positive myoclonus dystonia.
Mov Disord,
23(5):761-4,
2008.
Note: Sabine MeunierGeorge LourencoMarie VidailhetJournal ArticleUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): Adult,
Aged,
Cerebral Cortex/*physiopathology,
Dystonic Disorders/diagnosis/genetics/*physiopathology,
Electrophysiology,
Evoked Potentials,
Motor,
Female,
Genes,
Dominant,
Heterozygote,
Humans,
Male,
Middle Aged,
Neural Inhibition,
Reaction Time,
Reference Values,
Sarcoglycans/*genetics,
Synaptic Transmission,
Transcranial Magnetic Stimulation.
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E. Roze,
S. Betuing,
C. Deyts,
E. Marcon,
K. Brami-Cherrier,
C. Pages,
S. Humbert,
K. Merienne,
and J. Caboche.
Mitogen- and stress-activated protein kinase-1 deficiency is involved in expanded-huntingtin-induced transcriptional dysregulation and striatal death.
Faseb J,
2008.
Note: Journal articleofficial publication of the Federation of American Societies for Experimental Biology.
[WWW]
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F. Sedel,
J. M. Saudubray,
E. Roze,
Y. Agid,
and M. Vidailhet.
Movement disorders and inborn errors of metabolism in adults: a diagnostic approach.
J Inherit Metab Dis,
31(3):308-18,
2008.
Note: Journal ArticleReviewNetherlands.
[WWW]
Keyword(s): Adolescent,
Adult,
Amino Acids/metabolism,
Copper/metabolism,
Energy Metabolism,
Gangliosidosis,
GM1/diagnosis,
Humans,
Iron/metabolism,
Metabolism,
Inborn Errors/*diagnosis,
Movement Disorders/*diagnosis,
Neurotransmitter Agents/biosynthesis.
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J. M. Trocello,
P. Zanotti-Fregonara,
E. Roze,
E. Apartis,
A. P. Legrand,
M. O. Habert,
J. Y. Devaux,
and M. Vidailhet.
Dopaminergic deficit is not the rule in orthostatic tremor.
Mov Disord,
23(12):1733-8,
2008.
Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): Aged,
Brain Mapping,
Dopamine/*deficiency/physiology,
Electromyography,
Female,
Humans,
Male,
Middle Aged,
Tomography,
Emission-Computed,
Single-Photon/methods,
Tremor/drug therapy/*physiopathology/radionuclide imaging,
Tropanes/diagnostic use.
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P. Zanotti-Fregonara,
M. Vidailhet,
A. Kas,
L. J. Ozelius,
F. Clot,
E. Hindie,
L. Ravasi,
J. Y. Devaux,
and E. Roze.
[(123)I]-FP-CIT and [(99m)Tc]-HMPAO single photon emission computed tomography in a new sporadic case of rapid-onset dystonia-parkinsonism.
J Neurol Sci,
273(1-2):148-51,
2008.
Note: Journal ArticleNetherlands.
[WWW]
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E. Apartis,
E. Roze,
F. Clot,
I. Guyon-Marechal,
S. Thobois,
C. Tranchant,
P. Damier,
Y. Beaugendre,
A. Durr,
and M. Vidailhet.
Clinical and electrophysiological phenotype of myoclonus dystonia due to epsilon sarcoglycan gene mutations.
Mov Disord,
22:S5-S5,
2007.
Note: Suppl. 16.
[WWW]
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P. Bounolleau,
E. Apartis,
D. Ducreux,
Y. Beaugendre,
M. C. Lavallard-Rousseau,
F. Bourdain,
P. Dupont,
L. Carluer,
L. Verdure,
M. Vidailhet,
and E. Roze.
Propriospinal myoclonus: Report of seven new cases and literature review.
Mov Disord,
22:S138-S139,
2007.
Note: Suppl. 16.
[WWW]
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V. Cochen-De Cock,
M. Vidailhet,
E. Roze,
Y. Agid,
J. Willer,
J. Derenne,
and P. Arnulf.
Restoration of normal motor control in Parkinson's disease during REM sleep.
Sleep,
30:A291-A291,
2007.
Note: Suppl. S.
[WWW]
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V. C. De Cock,
A. Lannuzel,
S. Verhaeghe,
E. Roze,
M. Ruberg,
J. P. Derenne,
J. C. Willer,
M. Vidailhet,
and I. Arnulf.
REM sleep behavior disorder in patients with guadeloupean parkinsonism, a tauopathy.
Sleep,
30(8):1026-32,
2007.
Note: Journal ArticleUnited States.
[WWW]
Keyword(s): Aged,
Dementia/chemically induced/diagnosis,
Diagnosis,
Differential,
Disability Evaluation,
Dreams/drug effects,
Fatty Alcohols/*toxicity,
Female,
Fruit/*toxicity,
Guadeloupe,
Humans,
Lactones/*toxicity,
Male,
Mesencephalon/drug effects,
Middle Aged,
Motor Activity/drug effects,
Neurologic Examination/drug effects,
Parkinson Disease/diagnosis,
Parkinsonian Disorders/*chemically induced/diagnosis,
Polysomnography/drug effects,
Prospective Studies,
REM Sleep Behavior Disorder/*chemically induced/diagnosis,
Sleep-Wake Transition Disorders/chemically induced/diagnosis,
Supranuclear Palsy,
Progressive/chemically induced/diagnosis,
Tauopathies/*chemically induced/diagnosis.
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V. C. De Cock,
M. Vidailhet,
S. Leu,
A. Texeira,
E. Apartis,
A. Elbaz,
E. Roze,
J. C. Willer,
J. P. Derenne,
Y. Agid,
and I. Arnulf.
Restoration of normal motor control in Parkinson's disease during REM sleep.
Brain,
130(Pt 2):450-6,
2007.
Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglanda journal of neurology.
[WWW]
Keyword(s): Adult,
Dreams,
Electromyography/methods,
Facial Expression,
Female,
Humans,
Male,
Middle Aged,
*Movement,
Parkinson Disease/physiopathology/*psychology,
Polysomnography,
REM Sleep Behavior Disorder/*etiology/physiopathology/psychology,
Sleep,
REM,
Speech,
Video Recording.
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E. Guettard,
M. F. Portnoi,
B. Keren,
S. Rossignol,
S. Leu,
I. El Kamel,
E. Apartis,
M. Vidailhet,
and E. Roze.
Myoclonus dystonia and Silver-Russell syndrome in a patient with a supernumerary ring chromosome 7.
J Neurol,
254:92-93,
2007.
Note: Suppl. 3.
[WWW]
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K. Kinugawa,
E. Roze,
I. Mari,
J. F. Lepeintre,
S. Leu,
F. Heran,
and M. Vidailhet.
Subacute dopa responsive parkinsonism and hypersomnia after successful surgical treatment of aqueductal stenosis.
J Neurol,
254:93-93,
2007.
Note: Suppl. 3.
[WWW]
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S. Leu-Semenescu,
E. Roze,
M. Vidailhet,
A. P. Legrand,
J. M. Trocello,
V. Cochen,
S. Sangla,
and E. Apartis.
Myoclonus or tremor in orthostatism: an under-recognized cause of unsteadiness in Parkinson's disease.
Mov Disord,
22(14):2063-9,
2007.
Note: Journal ArticleUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): Adult,
Aged,
Aged,
80 and over,
Electromyography,
Female,
Humans,
Hypotension,
Orthostatic/*etiology,
Male,
Middle Aged,
Muscle Rigidity/*etiology,
Myoclonus/*complications,
Parkinson Disease/*physiopathology,
Retrospective Studies,
Tremor/*complications.
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E. Roze,
E. Apartis,
M. Vidailhet,
V. Cochen,
Y. Beaugendre,
J. M. Trocello,
P. Lasjaunias,
and D. Ducreux.
Propriospinal myoclonus: Utility of magnetic resonance diffusion tensor imaging and fiber tracking.
Mov Disord,
22(10):1506-9,
2007.
Note: Journal ArticleUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
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E. Roze,
E. Apartis,
M. Vidailhet,
V. Cochen,
Y. Beaugendre,
J. M. Trocello,
P. Lasjaunias,
and D. Ducreux.
Propriospinal myoclonus: utility of magnetic resonance diffusion tensor imaging and fibre tracking.
J Neurol,
254:15-15,
2007.
Note: Suppl. 3.
[WWW]
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E. Roze,
E. Apartis,
M. Vidailhet,
V. Cochen,
Y. Beaugendre,
J. M. Trocello,
P. Lasjaunias,
and D. Ducreux.
Steroid responsive propriospinal myoclonus associated with antithyroid antibodies.
Mov Disord,
22:S139-S139,
2007.
Note: Suppl. 16.
[WWW]
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E. Roze,
C. Azuar,
C. Menuel,
J. Haberle,
and R. Guillevin.
Usefulness of magnetic resonance spectroscopy in urea cycle disorders.
Pediatr Neurol,
37(3):222-5,
2007.
Note: Journal ArticleUnited States.
[WWW]
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E. Roze,
V. Cochen,
S. Sangla,
T. Bienvenu,
A. Roubergue,
S. Leu-Semenescu,
and M. Vidaihet.
Rett syndrome: an overlooked diagnosis in women with stereotypic hand movements, psychomotor retardation, Parkinsonism, and dystonia?.
Mov Disord,
22(3):387-9,
2007.
Note: Case ReportsJournal ArticleUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): Dystonia/etiology,
Female,
*Hand,
Humans,
Middle Aged,
Motor Skills Disorders/etiology,
Movement/*physiology,
Parkinson Disease/etiology,
Rett Syndrome/*diagnosis/*physiopathology.
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V. Cochen De Cock,
F. Bourdain,
E. Apartis,
J. M. Trocello,
E. Roze,
and M. Vidailhet.
Interictal myoclonus with paroxysmal kinesigenic dyskinesia.
Mov Disord,
21(9):1533-5,
2006.
Note: Case ReportsJournal ArticleUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): Adolescent,
Anticonvulsants/therapeutic use,
Cerebral Cortex/drug effects/physiopathology,
Choreatic Disorders/*diagnosis/drug therapy/physiopathology,
Dominance,
Cerebral/physiology,
Electroencephalography/drug effects,
Epilepsies,
Myoclonic/*diagnosis/drug therapy/physiopathology,
Humans,
Kinesthesis/drug effects/*physiology,
Male,
Neurologic Examination/drug effects.
-
E. Roze,
M. C. Coelho-Braga,
D. Gayraud,
A. P. Legrand,
J. M. Trocello,
G. Fenelon,
V. Cochen,
N. Patte,
F. Viallet,
M. Vidailhet,
P. Pollak,
and E. Apartis.
Head tremor in Parkinson's disease.
Mov Disord,
21(8):1245-8,
2006.
Note: Journal ArticleUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): *Head Movements,
Humans,
Parkinson Disease/*diagnosis/physiopathology,
Posture,
Rotation,
Supine Position,
Tremor/*etiology,
Videotape Recording.
-
E. Roze,
S. Navarro,
P. Cornu,
M. L. Welter,
and M. Vidailhet.
Deep brain stimulation of the globus pallidus for generalized dystonia in GM1 Type 3 gangliosidosis: technical case report.
Neurosurgery,
59(6):E1340;-discussion,
2006.
Note: Case ReportsJournal ArticleResearch Support, Non-U.S. Gov'tTechnical ReportUnited States.
[WWW]
Keyword(s): Adult,
Deep Brain Stimulation/*methods,
Dystonia/*etiology/*therapy,
Female,
Gangliosidosis,
GM1/*complications/*therapy,
Globus Pallidus,
Humans,
Treatment Outcome.
-
E. Roze,
M. Vidailhet,
N. Blau,
L. B. Moller,
D. Doummar,
T. B. de Villemeur,
and A. Roubergue.
Long-term follow-up and adult outcome of 6-pyruvoyl-tetrahydropterin synthase deficiency.
Mov Disord,
21(2):263-6,
2006.
Note: Case ReportsJournal ArticleResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): Adolescent,
Adult,
Antiparkinson Agents/therapeutic use,
Athetosis/*diagnosis/drug therapy/enzymology,
Child,
Child,
Preschool,
Chorea/*diagnosis/drug therapy/enzymology,
Dose-Response Relationship,
Drug,
Dystonia/*diagnosis/drug therapy/enzymology,
Female,
Follow-Up Studies,
Humans,
Infant,
Infant,
Newborn,
Levodopa/therapeutic use,
Long-Term Care,
Muscle Hypotonia/*diagnosis/drug therapy/enzymology,
Neurologic Examination,
Phenylketonurias/*diagnosis/drug therapy/enzymology,
Phosphorus-Oxygen Lyases/*deficiency,
Pterins/*metabolism,
Treatment Outcome.
-
S. Tezenas du Montcel,
F. Clot,
M. Vidailhet,
E. Roze,
P. Damier,
C. P. Jedynak,
A. Camuzat,
A. Lagueny,
L. Vercueil,
D. Doummar,
L. Guyant-Marechal,
J. L. Houeto,
G. Ponsot,
S. Thobois,
M. A. Cournelle,
A. Durr,
F. Durif,
B. Echenne,
D. Hannequin,
C. Tranchant,
and A. Brice.
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes.
J Med Genet,
43(5):394-400,
2006.
Note: French Dystonia NetworkJournal ArticleResearch Support, Non-U.S. Gov'tEngland.
[WWW]
Keyword(s): Adolescent,
Adult,
Aged,
Child,
Child,
Preschool,
Choreatic Disorders/diagnosis/genetics,
Chromosomes,
Human,
Pair 7,
Cohort Studies,
DNA Mutational Analysis,
Dystonic Disorders/*diagnosis/genetics,
Female,
France,
Genetic Screening,
Humans,
Infant,
Male,
Middle Aged,
Molecular Chaperones/genetics,
*Mutation,
Myoclonus/*diagnosis/genetics,
Phenotype,
Sarcoglycans/*genetics,
Syndrome.
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E. Roze,
E. Paschke,
N. Lopez,
T. Eck,
K. Yoshida,
A. Maurel-Ollivier,
D. Doummar,
C. Caillaud,
D. Galanaud,
T. Billette de Villemeur,
M. Vidailhet,
and A. Roubergue.
Dystonia and parkinsonism in GM1 type 3 gangliosidosis.
Mov Disord,
20(10):1366-9,
2005.
Note: Case ReportsJournal ArticleResearch Support, Non-U.S. Gov'tReviewUnited Statesofficial journal of the Movement Disorder Society.
[WWW]
Keyword(s): Adolescent,
Adult,
Alleles,
Body Height,
Bone Diseases,
Developmental/radiography,
Dystonia/diagnosis/*etiology,
Exons/genetics,
Female,
Gangliosidosis,
GM1/*complications/diagnosis/genetics,
Humans,
Parkinsonian Disorders/*etiology,
Point Mutation/genetics,
Videotape Recording,
beta-Galactosidase/deficiency/genetics.
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E. Roze,
D. Gervais,
S. Demeret,
H. Ogier de Baulny,
J. Zittoun,
J. F. Benoist,
G. Said,
C. Pierrot-Deseilligny,
and F. Bolgert.
Neuropsychiatric disturbances in presumed late-onset cobalamin C disease.
Arch Neurol,
60(10):1457-62,
2003.
Note: Clinical TrialJournal ArticleUnited States.
[WWW]
Keyword(s): Adolescent,
Adult,
Brain/pathology,
Cobamides/metabolism,
Female,
Fibroblasts/metabolism,
Homocysteine/blood/urine,
Humans,
Mental Disorders/*etiology/pathology/*psychology,
Metabolism,
Inborn Errors/complications/metabolism/*psychology,
Methylmalonic Acid/blood/urine,
Nervous System Diseases/*etiology/pathology/*psychology,
Sural Nerve/pathology,
Vitamin B 12/*analogs & derivatives/*metabolism.
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Last modified: Thu May 6 18:23:30 2010
Author: schwartz.
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