Long-Term Observations of Patients with Infantile Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1)-Reference-Cited by-同舟云学术

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Long-Term Observations of Patients with Infantile Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1)

Published:2004-06 Issue:3 Volume:35 Page:174-182
ISSN:0174-304X
Container-title:Neuropediatrics
language:de
Short-container-title:Neuropediatrics

Author:

Rudnik-Schöneborn S.,Stolz P.,Varon R.,Grohmann K.,Schächtele M.,Ketelsen U.-P.,Stavrou D.,Kurz H.,Hübner C.,Zerres K.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2004-820994.pdf

Cited by 57 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Disease Mechanisms and Therapeutic Approaches in SMARD1—Insights from Animal Models and Cell Models;Biomedicines;2024-04-11

2. ABT1 modifies SMARD1 pathology via interactions with IGHMBP2 and stimulation of ATPase and helicase activity;JCI Insight;2023-01-24

3. Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders;Neurological Research and Practice;2022-01-04

4. Spinal muscular atrophy with respiratory distress type 1 (smard1): a rare cause of hypotonia, diaphragmatic weakness, and respiratory failure in infants;The Turkish Journal of Pediatrics;2022

5. Defining the optimal dose and therapeutic window in SMA with respiratory distress type I model mice, FVB/NJ-Ighmpb2;Molecular Therapy - Methods & Clinical Development;2021-12

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