Matthias Schilling

Muenster, NW, Germany

Last Updated: 09/26/2026

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Found 24 publications

Disease modifying treatment of hereditary transthyretin amyloidosis with polyneuropathy in Germany - expert consensus of the German society of amyloid diseases (DGAK) and the German neurological society (DGN).

Disease modifying treatment of hereditary transthyretin amyloidosis with polyneuropathy in Germany - expert consensus of the German society of amyloid diseases (DGAK) and the German neurological society (DGN).

Journal: Neurological research and practice

Published: May 27, 2026

Contactin-associated protein 2 autoantibodies can be associated with multifocal motor-like neuropathy: a case report.

Contactin-associated protein 2 autoantibodies can be associated with multifocal motor-like neuropathy: a case report.

Journal: Therapeutic advances in neurological disorders

Published: April 13, 2023

de novo hATTR amyloidosis after domino transplantation of a donor's liver: a case report for the use of Patisiran

de novo hATTR amyloidosis after domino transplantation of a donor's liver: a case report for the use of Patisiran

Journal: Zeitschrift fur Gastroenterologie

Published: May 09, 2022

Gene therapy options for hereditary transthyretin-related amyloidosis

Gene therapy options for hereditary transthyretin-related amyloidosis

Journal: Der Nervenarzt

Published: March 08, 2022

Detecting myasthenia gravis as a cause of unclear dysphagia with an endoscopic tensilon test.

Detecting myasthenia gravis as a cause of unclear dysphagia with an endoscopic tensilon test.

Journal: Therapeutic advances in neurological disorders

Published: May 15, 2021

Genome silencer therapy leading to 'regression' of cardiac amyloid load on cardiovascular magnetic resonance: a case report.

Genome silencer therapy leading to 'regression' of cardiac amyloid load on cardiovascular magnetic resonance: a case report.

Journal: European heart journal. Case reports

Published: January 19, 2021

Chance or challenge, spoilt for choice? New recommendations on diagnostic and therapeutic considerations in hereditary transthyretin amyloidosis with polyneuropathy: the German/Austrian position and review of the literature.

Chance or challenge, spoilt for choice? New recommendations on diagnostic and therapeutic considerations in hereditary transthyretin amyloidosis with polyneuropathy: the German/Austrian position and review of the literature.

Journal: Journal of neurology

Published: May 07, 2020

Quality of life outcomes in APOLLO, the phase 3 trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosis.

Quality of life outcomes in APOLLO, the phase 3 trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosis.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Published: March 06, 2020

Comparing Plasma Exchange to Escalated Methyl Prednisolone in Refractory Multiple Sclerosis Relapses.

Comparing Plasma Exchange to Escalated Methyl Prednisolone in Refractory Multiple Sclerosis Relapses.

Journal: Journal of clinical medicine

Published: December 03, 2019

Transthyretin Familial Amyloid Polyneuropathy - Disease Profile of a Multisystem Disorder

Transthyretin Familial Amyloid Polyneuropathy - Disease Profile of a Multisystem Disorder

Journal: Deutsche medizinische Wochenschrift (1946)

Published: April 17, 2018

Transthyretin Familial Amyloid Polyneuropathy - Disease Profile of a Multisystem Disorder

Transthyretin Familial Amyloid Polyneuropathy - Disease Profile of a Multisystem Disorder

Journal: Deutsche medizinische Wochenschrift (1946)

Published: March 16, 2018

De novo hereditary (familial) amyloid polyneuropathy (FAP) in a FAP liver recipient.

De novo hereditary (familial) amyloid polyneuropathy (FAP) in a FAP liver recipient.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Published: April 25, 2017

Showing 1-12 of 24

Last Updated: 09/26/2026