T. Arthur

Type de document

Co-auteur

M.A. Willemsen

R.A. Wevers

B. Weschke

D. Webb

M.M. Verbeek

B.G. van Engelen

P. van Bogaert

J. Trounce

R. Tomlinson

P. Sykora

N. Simpson

E. Sheridan

T. Scheffner

H. Scheffer

I. Sandvig

C.M. Rouselle

C. Rauscher

B.T. Poll-The

A. Panzer

N.O. Nilsson

H. Mundy

M.E. Meuwissen

J. McMenamin

L. Martorell

A.D. Marina

G. Mancini

M.J. Lim

K. Leppig

M. Leferink

W.G. Leen

V Laugel

K. Lachlan

J. Klepper

S. Jayawant

H. Holthausen

T. Hofste

S. Grunewald

S. Gross

R.J. Forsyth

K. Farrell

A. Evangeliou

F. Ebinger

E. Donner

C.G. de Goede

J. Coldwell

P. Clayton

M.P. Champion

B. Chabrol

I. Carrilho

J. Bekhof

D. Ballhausen

N. Bahi-Buisson

Date

Source

Serveur académique Lausannois (1)

Mot-clé

nourisson (1) mutation (1) analyse (1) gène (1) famille (1) âge (1) enfant (1) adulte (1) jeune (1) Case (1) Phenotype (1) Transportation (1) Symptoms (1) Spine--Puncture (1) Series (1) Scarcity (1) Physicians (1) Patients (1) Movement disorders (1) Mental retardation (1) Human beings (1) Ketogenic diet (1) Grammar, Comparative and general--Case (1) Glucose (1) Families (1) Epilepsy (1) Cerebrospinal fluid (1) Case (1) Carbohydrates--Metabolism (1) Brain (1)

Documents écrit par T. Arthur (1) | parle de T. Arthur (3)

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.

W.G. Leen et al. (2010)