Said Hashemolhosseini
Erlangen, BY 91054, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 27 publications
Crosstalk among canonical Wnt and Hippo pathway members in skeletal muscle and at the neuromuscular junction.
Journal: Neural regeneration research
Published: April 15, 2024
The impact of canonical Wnt transcriptional repressors TLE3 and TLE4 on postsynaptic transcription at the neuromuscular junction.
Journal: Frontiers in molecular neuroscience
Published: December 22, 2023
Salbutamol repurposing ameliorates neuromuscular junction defects and muscle atrophy in Col6a1-/- mouse model of collagen VI-related myopathies.
Journal: Clinical and translational medicine
Published: December 22, 2023
In Skeletal Muscle Fibers, Protein Kinase Subunit CSNK2A1/CK2α Is Required for Proper Muscle Homeostasis and Structure and Function of Neuromuscular Junctions.
Journal: Cells
Published: October 31, 2022
The desmin mutation R349P increases contractility and fragility of stem cell-generated muscle micro-tissues.
Journal: Neuropathology and applied neurobiology
Published: July 27, 2021
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP syndrome) caused by a novel mutation in ADPRHL2 (AHR3).
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 04, 2021
Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine.
Journal: Acta neurologica Belgica
Published: August 07, 2020
Lack of Desmin in Mice Causes Structural and Functional Disorders of Neuromuscular Junctions.
Journal: Frontiers in molecular neuroscience
Published: May 29, 2020
Last Updated: 09/26/2026