|
Neuromuscular diseases
Citations 161-170 of 238 total displayed.
|
Past content
(since Jan 1998):
|
- Observations
Polymyositis Masquerading as Motor Neuron Disease
- Aisling Ryan; Azli M. Nor; Donal Costigan; Daragh Foley-Nolan; Ahmed El-Rafie; Michael A. Farrell; Orla Hardiman
Arch Neurol 2003; 60: 1001-1003.
[Abstract]
[Full text]
[PDF]
- Original Contributions
Disease Course of Charcot-Marie-Tooth Disease Type 2: A 5-Year Follow-up Study
- Laurien L. Teunissen; Nicolette C. Notermans; Hessel Franssen; Baziel G. M. van Engelen; Frank Baas; John H. J. Wokke
Arch Neurol 2003; 60: 823-828.
[Abstract]
[Full text]
[PDF]
- Images in Neurology
Kennedy Disease: Avoiding Misdiagnosis
- Konstantinos Paparounas; Anna Gotsi; Maria Syrrou; Nikolaos Akritidis
Arch Neurol 2003; 60: 893-894.
[Extract]
[Full text]
[PDF]
- Observations
Congenital Myasthenic Syndrome With Episodic Apnea in Patients Homozygous for a CHAT Missense Mutation
- Simone Kraner; Iris Laufenberg; Hans M. Straßburg; Joern P. Sieb; Ortrud K. Steinlein
Arch Neurol 2003; 60: 761-763.
[Abstract]
[Full text]
[PDF]
- Editorials
Genetics of Charcot-Marie-Tooth Disease
- David E. Pleasure
Arch Neurol 2003; 60: 481-482.
[Extract]
[Full text]
[PDF]
- Original Contributions
A Clustering of Conjugal Amyotrophic Lateral Sclerosis in Southeastern France
- Philippe Corcia; Helene-Farnase Jafari-Schluep; Dominique Lardillier; Hassan Mazyad; Pieric Giraud; Pierre Clavelou; Jean Pouget; William Camu
Arch Neurol 2003; 60: 553-557.
[Abstract]
[Full text]
[PDF]
- Observations
Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene
- Nazha Birouk; Hamid Azzedine; Odile Dubourg; Marie-Paule Muriel; Ali Benomar; Tarik Hamadouche; Thierry Maisonobe; Reda Ouazzani; Alexis Brice; Mohamed Yahyaoui; Taïb Chkili; Eric Le Guern
Arch Neurol 2003; 60: 598-604.
[Abstract]
[Full text]
[PDF]
- Observations
Transient, Recurrent, White Matter Lesions in X-linked Charcot-Marie-Tooth Disease With Novel Connexin 32 Mutation
- C. Oliver Hanemann; Carsten Bergmann; Jan Senderek; Klaus Zerres; Ann-Dorte Sperfeld
Arch Neurol 2003; 60: 605-609.
[Abstract]
[Full text]
[PDF]
- Neurological Reviews
Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations: A Review
- Michaela Auer-Grumbach; Peter De Jonghe; Kristien Verhoeven; Vincent Timmerman; Klaus Wagner; Hans-Peter Hartung; Garth A. Nicholson
Arch Neurol 2003; 60: 329-334.
[Abstract]
[Full text]
[PDF]
- Original Contributions
Development of Generalized Disease at 2 Years in Patients With Ocular Myasthenia Gravis
- Mark J. Kupersmith; Robert Latkany; Peter Homel
Arch Neurol 2003; 60: 243-248.
[Abstract]
[Full text]
[PDF]
|
|