H. Goebel

发表

Macrophages in multiple sclerosis.

W. Brück, H. Lassmann, H. Kretzschmar, 1996, Immunobiology.

Alcohol-related acute axonal polyneuropathy: a differential diagnosis of Guillain-Barré syndrome.

J. Wöhrle, K. Spengos, M. Hennerici, 1998, Archives of neurology.

Consequences of mutations within the C terminus of the FHL1 gene

H. Goebel, B. Schoser, C. Windpassinger, 2009, Neurology.

A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population

H. Reichmann, H. Goebel, Hanns Lochmüller, 2002, Neuromuscular Disorders.

A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.

N. Drouot, M. Koenig, M. Gribaa, 2007, Brain : a journal of neurology.

Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: Muscle biopsy and autopsy findings, biochemical and molecular genetic studies

S. Dimauro, G. Sevlever, A. Taratuto, 2010, Neuromuscular Disorders.

Post-COVID syndrome is associated with capillary alterations, macrophage infiltration and distinct transcriptomic signatures in skeletal muscles

F. Heppner, M. Landthaler, C. Scheibenbogen, 2023, medRxiv.

Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis

D. Pongratz, K. Ricker, W. Müller-Felber, 1999, Neuromuscular Disorders.