Ghent University Academic Bibliography

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Your filters: cql: author="CEUTERICK, C" or (type any "bookEditor issueEditor" and editor="CEUTERICK, C")

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- Journal Article
- A1
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2

Kristien Verhoeven, KG CLAEYS, S ZUCHNER, JM SCHRODER, J WEIS, C CEUTERICK, A JORDANOVA, E NELIS, Els De Vriendt, M VAN HUL, et al.

(2006) BRAIN. 129. p.2093-2102
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Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia

G Van Goethem, JJ Martin, Bart Dermaut (UGent) , A Löfgren, A Wibail, D Ververken, P Tack, I Dehaene, M Van Zandijcke, M Moonen, et al.

(2003) NEUROMUSCULAR DISORDERS. 13(2). p.133-142
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- Journal Article
- A1
CasprI/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies.

K VENKEN, J MEULEMAN, J IROBI, C CEUTERICK, R MARTINI, P DE JONGHE and V TIMMERMAN

(2001) NEUROREPORT. 12(11). p.2609-2614
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- Journal Article
- A1
INTERMEDIATE SYNDROME DUE TO PROLONGED PARATHION POISONING.

Jan De Bleecker (UGent) , Dirk Vogelaers (UGent) , C CEUTERICK, K VANDENNEUCKER, Jan Willems and Jacques De Reuck

(1992) ACTA NEUROLOGICA SCANDINAVICA. 86(4). p.421-424
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- Journal Article
- A1
BECKER-TYPE MUSCULAR-DYSTROPHY - REPORT OF A FAMILY WITH ONE POSTMORTEM STUDY.

JJ MARTIN, Juliaan Leroy (UGent) , C CEUTERICK, U LUBKE, E VANBUGGENHOUT, J VANVUCHELEN and C VANBROECKHOVEN

(1992) CLINICAL NEUROLOGY AND NEUROSURGERY.
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- Conference Paper
- C1
Dermatomyositis with paracrystalline inclusions and polymicrogyria in two sisters

Jan De Bleecker (UGent) , Jacques De Reuck, J MARTIN, C CEUTERICK, Dietbrand Carton and Juliaan Leroy (UGent)

(1988) Clinical neuropathology. 7. p.158-158
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- Conference Paper
- C1
Polymicrogyria and dermatomyositis in two sisters

Jacques De Reuck, Dietbrand Carton, J MARTIN, C CEUTERICK, Jan De Bleecker (UGent) and Juliaan Leroy (UGent)

(1987) ACTA NEUROLOGICA BELGICA. 87. p.172-172

Academic Bibliography

MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2

Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia

CasprI/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies.

INTERMEDIATE SYNDROME DUE TO PROLONGED PARATHION POISONING.

BECKER-TYPE MUSCULAR-DYSTROPHY - REPORT OF A FAMILY WITH ONE POSTMORTEM STUDY.

Dermatomyositis with paracrystalline inclusions and polymicrogyria in two sisters

Polymicrogyria and dermatomyositis in two sisters

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