J.A. Lobrinus

Discipline

Sociologie (1) Psychologie (1) Sciences de l'information et de la communication (1) Education (1)

Type de document

Articles (12)

Co-auteur

Date

Source

Mot-clé

Human beings (10) Older people (8) Patients (6) Patients (6) adulte (5) Case (5) Grammar, Comparative and general--Case (5) Case (5) adulte (5) Treatment (4) Muscles (4) mutation (3) analyse (3) gène (3) Diagnosis (3) Swiss (3) Muscular dystrophy (3) Muscles--Diseases (3) Magnetic resonance imaging (3) Diagnosis (3) Analysis (3) Mutation (3) Magnetic resonance imaging (3) puits (2) thérapie (2) âge (2) Methods (2) Therapeutics (2) Mice (2) Fibers (2)

Documents écrit par J.A. Lobrinus (12) | parle de J.A. Lobrinus (0)

Prevalence of large vessel vasculitis in ANCA-associated vasculitis: a retrospective cohort study.
Y. Coattrenec et al.
Intimomedial mucoid arterial degeneration, a rare arterial disorder of forensic significance.
K. Wiskott et al.
Fatal subarachnoid hemorrhage following ischemia in vertebrobasilar dolichoectasia.
A.A. Sokolov et al.
Dysferlinopathy in Switzerland: clinical phenotypes and potential founder effects.
J.A. Petersen et al. (2015)
Solitary Neurofibroma Of The Spermatic Cord: A Case Report.
J. Boto et al. (2015)
Assessing dystrophies and other muscle diseases at the nanometer scale by atomic force microscopy.
R.W. van Zwieten et al. (2014)
Functional and histopathological identification of the respiratory failure in a DMSXL transgenic mouse model of myotonic dystrophy.
P.A. Panaite et al. (2013)
Schwannoma of the palmar cutaneous nerve: electrodiagnosis with radiologic and pathologic correlations.
A. Zekeridou et al.
Successful heart and liver transplantation in a Swiss patient with Glu89Lys transthyretin amyloidosis.
J. Niederhauser et al. (2011)
Chemotherapy is successful in sporadic late onset nemaline myopathy (SLONM) with monoclonal gammopathy.
J. Novy et al.
Marked hemiatrophy in carriers of Duchenne muscular dystrophy.
S. Rajakulendran et al. (2010)
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy.
M. Dunand et al.