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DGM 2023
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DE
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Dr. Andreas Hentschel
Dortmund / DE
Leibniz-Institut für Analytische Wissenschaften – ISAS – e.V.
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Date
Further involvements
22/03/2023
Poster
P 62
Impaired proteostasis and unfolded-protein response activation in skeletal muscle of systemic sclerosis patient
Pathophysiologie und molekulare Mechanismen, Varia
22/03/2023
Poster
P 4
Periostin level in sporadic inclusion body myositis: a study of blood and muscle
Biomarker - molekular, klinisch, digital, Pathophysiologie und molekulare Mechanismen
22/03/2023
Poster
P 71
Molecular profiling of skeletal muscle of patients with Late Onset Pompe Disease
Pathophysiologie und molekulare Mechanismen, Varia
22/03/2023
Poster
P 81
Phenotyping, histopathological and biochemical analysis of a calpain-deficient mouse model
Pathophysiologie und molekulare Mechanismen, Varia
23/03/2023
15:25
–
15:30
4 Min.
1 Min.
Orales Poster
P 4
Periostin level in sporadic inclusion body myositis: a study of blood and muscle
Biomarker - molekular, klinisch, digital, Pathophysiologie und molekulare Mechanismen
24/03/2023
13:33
–
13:45
12 Min.
0 Min.
Freier Vortrag
FV 21
First clinical and myopathological description of a congenital myopathy based on a homozygous variant in
TNNI2
Case reports, Pathophysiologie und molekulare Mechanismen
24/03/2023
15:45
–
15:50
4 Min.
1 Min.
Orales Poster
P 62
Impaired proteostasis and unfolded-protein response activation in skeletal muscle of systemic sclerosis patient
Pathophysiologie und molekulare Mechanismen, Varia
24/03/2023
16:00
–
16:10
10 Min.
0 Min.
Freier Vortrag
FV 23
Bi-allelic variants of FILIP1 cause a congenital syndrome with a range of myopathic and neurological manifestations and facial dysmorphisms
Pathophysiologie und molekulare Mechanismen, Varia
24/03/2023
16:10
–
16:20
10 Min.
0 Min.
Freier Vortrag
FV 24
Molecular deciphering of disease processes in SLC12A6-associated sensorimotor neuropathy
Biomarker - molekular, klinisch, digital, Pathophysiologie und molekulare Mechanismen
24/03/2023
16:20
–
16:30
10 Min.
0 Min.
Freier Vortrag
FV 25
Erweiterung des Spektrums
BICD2
-assoziierter Erkrankungen – Identifikation neuer genetischer Varianten mit Myopathie sowie assoziierter Markerproteine
Biomarker - molekular, klinisch, digital, Pathophysiologie und molekulare Mechanismen
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