Spinal muscular atrophy with respiratory distress type 1 (smard1): a rare cause of hypotonia, diaphragmatic weakness, and respiratory failure in infants-Reference-Cited by-同舟云学术

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Spinal muscular atrophy with respiratory distress type 1 (smard1): a rare cause of hypotonia, diaphragmatic weakness, and respiratory failure in infants

Published:2022 Issue:2 Volume:64 Page:364
ISSN:0041-4301
Container-title:The Turkish Journal of Pediatrics
language:
Short-container-title:TurkJPediatr

Author:

Pekuz Serdar,Güzin Yiğithan,Sarıtaş Serdar,Kırbıyık Özgür,Ünalp Aycan,Yılmaz Ünsal

Abstract

Publisher

The Turkish Journal of Pediatrics

Subject

Pediatrics, Perinatology and Child Health

Cited by 5 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. Diaphragmatic Paralysis;Smith's Recognizable Patterns of Human Deformation;2025

2. The Clinical Heterogeneity of Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1)—A Report of Three Cases, Including Twins;Genes;2024-07-30

3. Case report: Heterozygous variation in the IGHMBP2 gene leading to spinal muscular atrophy with respiratory distress type 1;Frontiers in Neurology;2024-05-30

4. Neuromuscular problems of the critically Ill neonate and child;Seminars in Pediatric Neurology;2024-04

5. Exploring the relationship between IGHMBP2 gene mutations and spinal muscular atrophy with respiratory distress type 1 and Charcot-Marie-Tooth disease type 2S: a systematic review;Frontiers in Neuroscience;2023-11-17

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