C. Hendrich

发表

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

Ewout J N Groen, Machiel J Zwarts, Fernando Rivadeneira, 2009, Nature Genetics.

Linking neuron and skin: Matrix metalloproteinases in amyotrophic lateral sclerosis (ALS)

A. Ludolph, J. Dorst, H. Tumani, 2009, Journal of the Neurological Sciences.

Linking neuron and skin: matrix metalloproteinases in amyotrophic lateral sclerosis

A. Ludolph, J. Dorst, H. Tumani, 2009 .

MMP-2 and MMP-9 are elevated in spinal cord and skin in a mouse model of ALS

A. Ludolph, J. Dorst, H. Tumani, 2010, Journal of the Neurological Sciences.

Patients with elevated triglyceride and cholesterol serum levels have a prolonged survival in amyotrophic lateral sclerosis

J. Kassubek, A. Ludolph, J. Dorst, 2011, Journal of Neurology.

Small-fiber neuropathy in patients with ALS

I. Katona, G. Müller-Newen, C. Sommer, 2011, Neurology.

The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases

A. Ludolph, J. Epplen, A. Sperfeld, 2013, neurogenetics.

Proteome analysis reveals candidate markers of disease progression in amyotrophic lateral sclerosis (ALS)

M. Pfeifle, A. Ludolph, J. Dorst, 2010, Neuroscience Letters.

Phenotypic spectrum in recessive STING-associated vasculopathy with onset in infancy: Four novel cases and analysis of previously reported cases

D. Steinemann, C. Klemann, D. Jonigk, 2022, Frontiers in Immunology.

Case report: Early-onset Parkinson's disease with initial spastic paraparesis and hyperreflexia caused by compound heterozygous PRKN-gene exon 2 and 4 deletions

G. Berding, F. Wegner, G. Höglinger, 2022, Frontiers in Neurology.

The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases

A. Ludolph, J. Epplen, A. Sperfeld, 2013, neurogenetics.

An unusual presentation of Huntington’s disease

H. Frieling, S. Bleich, G. Berding, 2021, Clinical case reports.

The dynactin p150 subunit: cell biology studies of sequence changes found in ALS/MND and Parkinsonian Syndromes

P. Wong, T. Boeckers, A. Ludolph, 2013, Journal of Neural Transmission.

Acute Cerebrovascular Disease in the Young: The Stroke in Young Fabry Patients Study

G. Deuschl, A. Metz, D. Krieger, 2013, Stroke.

TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

J. Trojanowski, V. Lee, H. Kretzschmar, 2008, Archives of neurology.

Concentrations of beta-amyloid precursor protein processing products in cerebrospinal fluid of patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration

F. Mottaghy, A. Ludolph, H. Tumani, 2009, Journal of Neural Transmission.