Bertold Schrank

Wiesbaden, HE 65191, Germany

Last Updated: 09/26/2026

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Found 24 publications

End of life perspectives: a systematic survey of patients with amyotrophic lateral sclerosis

End of life perspectives: a systematic survey of patients with amyotrophic lateral sclerosis

Journal: Der Nervenarzt

Published: October 10, 2024

Different Patterns of Autoantibody Secretion by Peripheral Blood Mononuclear Cells in Autoimmune Nodopathies.

Different Patterns of Autoantibody Secretion by Peripheral Blood Mononuclear Cells in Autoimmune Nodopathies.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: August 22, 2024

5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2.

5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2.

Journal: Journal of neurology

Published: October 30, 2023

Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study.

Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study.

Journal: The Lancet regional health. Europe

Published: October 24, 2023

Improvements in Walking Distance during Nusinersen Treatment - A Prospective 3-year SMArtCARE Registry Study.

Improvements in Walking Distance during Nusinersen Treatment - A Prospective 3-year SMArtCARE Registry Study.

Journal: Journal of neuromuscular diseases

Published: December 24, 2022

A form of muscular dystrophy associated with pathogenic variants in JAG2.

A form of muscular dystrophy associated with pathogenic variants in JAG2.

Journal: American journal of human genetics

Published: June 04, 2021

A form of muscular dystrophy associated with pathogenic variants in JAG2.

A form of muscular dystrophy associated with pathogenic variants in JAG2.

Journal: American journal of human genetics

Published: November 30, 2020

Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease.

Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease.

Journal: Human mutation

Published: October 08, 2020

Novel variants broaden the phenotypic spectrum of PLEKHG5-associated neuropathies.

Novel variants broaden the phenotypic spectrum of PLEKHG5-associated neuropathies.

Journal: European journal of neurology

Published: October 02, 2020

FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic Data.

FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic Data.

Journal: Neurology. Genetics

Published: July 23, 2020

De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation.

De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation.

Journal: American journal of human genetics

Published: May 29, 2020

Effect of high-caloric nutrition on serum neurofilament light chain levels in amyotrophic lateral sclerosis.

Effect of high-caloric nutrition on serum neurofilament light chain levels in amyotrophic lateral sclerosis.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: March 31, 2020

Showing 1-12 of 24

Last Updated: 09/26/2026