MovDisordV3, France, Analysis, indexItem, Author.i, Thierry Billette De Villemeur

Thierry Bienvenu < Thierry Billette De Villemeur < Thierry Grandmougin

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 4.

Ident.	Authors (with country if any)	Title
000251 (2009)	Diane Doummar [France] ; Fabienne Clot [France] ; Marie Vidailhet [France] ; Alexandra Afenjar [France] ; Alexandra Durr [France] ; Alexis Brice [France] ; Cyril Mignot [France] ; Agnès Guet [France] ; Thierry Billette De Villemeur [France] ; Diana Rodriguez [France]	Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene
000360 (2006)	Emmanuel Roze [France] ; Marie Vidailhet [France] ; Nenad Blau [Suisse] ; Lisbeth Birk Moller [Danemark] ; Diane Doummar [France] ; Thierry Billette De Villemeur [France] ; Anne Roubergue [France]	Long‐term follow‐up and adult outcome of 6‐pyruvoyl‐tetrahydropterin synthase deficiency
000408 (2005)	Emmanuel Roze [France] ; Eduard Paschke [Autriche] ; Nathalie Lopez [France] ; Thomas Eck [Autriche] ; Kunihiro Yoshida [Japon] ; Annie Maurel-Ollivier [France] ; Diane Doummar [France] ; Catherine Caillaud [France] ; Damien Galanaud [France] ; Thierry Billette De Villemeur [France] ; Marie Vidailhet [France] ; Anne Roubergue [France]	Dystonia and parkinsonism in GM1 type 3 gangliosidosis
000430 (2004)	Anne Roubergue [France] ; Emmanuelle Apartis [France] ; Marie Vidailhet [France] ; Cyril Mignot [France] ; Anna Tullio-Pelet [France] ; Stanislas Lyonnet [France] ; Thierry Billette De Villemeur [France]	Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutation

List of associated KwdEn.i

Nombre de documents	Descripteur
4	Female
4	Humans
3	Adult
3	Nervous system diseases
2	Adolescent
2	Deficiency
2	Dystonia
2	Dystonia (diagnosis)
2	Infant
2	Point Mutation (genetics)
2	symptomatic dystonia
1	6‐pyruvoyl‐tetrahydropterin synthase deficiency
1	Adrenal Gland Diseases (complications)
1	Adrenal Gland Diseases (genetics)
1	Alleles
1	Antiparkinson Agents (therapeutic use)
1	Athetosis (diagnosis)
1	Athetosis (drug therapy)
1	Athetosis (enzymology)
1	Body Height
1	Bone Diseases, Developmental (radiography)
1	Child
1	Child, Preschool
1	Chorea (diagnosis)
1	Chorea (drug therapy)
1	Chorea (enzymology)
1	Choreoathetosis
1	DNA Mutational Analysis
1	Digestive system
1	Dose-Response Relationship, Drug
1	Dystonia (drug therapy)
1	Dystonia (enzymology)
1	Dystonia (etiology)
1	Electromyography
1	Esophageal Achalasia (complications)
1	Esophageal Achalasia (genetics)
1	Esophageal Achalasia (physiopathology)
1	Exons (genetics)
1	Follow-Up Studies
1	GM1 gangliosidosis
1	Galactosidase
1	Gangliosidosis, GM1 (complications)
1	Gangliosidosis, GM1 (diagnosis)
1	Gangliosidosis, GM1 (genetics)
1	Gastrointestinal Diseases (complications)
1	Gastrointestinal Diseases (genetics)
1	Gastrointestinal Diseases (physiopathology)
1	Gastrointestinal Motility (physiology)
1	Homovanillic Acid (metabolism)
1	Hydroxyindoleacetic Acid (metabolism)
1	Hyperphenylalaninemia
1	Infant, Newborn
1	Lacrimal Apparatus Diseases (complications)
1	Lacrimal Apparatus Diseases (genetics)
1	Levodopa (therapeutic use)
1	Lipids
1	Long term
1	Long-Term Care
1	Lysosomal storage disease
1	Malignant tumor
1	Muscle Hypotonia (diagnosis)
1	Muscle Hypotonia (drug therapy)
1	Muscle Hypotonia (enzymology)
1	Muscle Hypotonia (genetics)
1	Muscle Hypotonia (metabolism)
1	Muscle Hypotonia (physiopathology)
1	Mutation
1	Mutation (genetics)
1	Myoclonus
1	Myoclonus (complications)
1	Nerve Tissue Proteins
1	Neurologic Examination
1	Nuclear Pore Complex Proteins
1	Parkinsonian Disorders (etiology)
1	Parkinsonism
1	Phenylketonurias (diagnosis)
1	Phenylketonurias (drug therapy)
1	Phenylketonurias (enzymology)
1	Phosphorus-Oxygen Lyases (deficiency)
1	Prognosis
1	Proteins (genetics)
1	Pterins (metabolism)
1	Syndrome
1	Synthase
1	Tetrahydrobiopterin
1	Treatment Outcome
1	Tyrosine 3-Monooxygenase (genetics)
1	Videotape Recording
1	beta-Galactosidase (deficiency)
1	beta-Galactosidase (genetics)
1	beta‐galactosidase deficiency
1	beta‐galactosidosis
1	choreoathetosis
1	digestive dysmotility
1	lysosomal storage disorder
1	malignant hyperphenylalaninemia
1	myoclonus
1	parkinsonism
1	tetrahydrobiopterin deficiency
1	triple A syndrome

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/France/Analysis

HfdIndexSelect -h $EXPLOR_AREA/Data/France/Analysis/Author.i -k "Thierry Billette De Villemeur"

HfdIndexSelect -h $EXPLOR_AREA/Data/France/Analysis/Author.i  \
                -Sk "Thierry Billette De Villemeur" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/France/Analysis/biblio.hfd

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    France
   |étape=   Analysis
   |type=    indexItem
   |index=    Author.i
   |clé=    Thierry Billette De Villemeur
}}

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024

	Movement Disorders (revue) - Analysis (France) Index « Auteurs » - entrée « Thierry Billette De Villemeur »
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Movement Disorders (revue) - Analysis (France)Index « Auteurs » - entrée « Thierry Billette De Villemeur »

List of bibliographic references

List of associated KwdEn.i

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Thierry Billette De Villemeur »