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This paper is in the following e-collection/theme issue:

Non-Randomized Study Protocols and Methods (Non-eHealth) (1231) Epidemiology (253) Pediatrics (276) Birth Defects (21) Epidemiologic Studies and Surveys in Child Health (52) Screening and Early Diagnosis in Pediatrics (62) Developmental Problems (101)

Published on in Vol 10, No 8 (2021): August

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/28619, first published .
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Mucopolysaccharidosis Type I Disease Prevalence Among Patients With Idiopathic Short Stature in Saudi Arabia: Protocol for a Multicenter Cross-sectional Study

Mucopolysaccharidosis Type I Disease Prevalence Among Patients With Idiopathic Short Stature in Saudi Arabia: Protocol for a Multicenter Cross-sectional Study

Authors of this article:

Danyah Alsafadi1 Author Orcid Image ;   Aly Ezzat2 Author Orcid Image ;   Fatima Altamimi3 Author Orcid Image ;   Marwan ElBagoury2 Author Orcid Image ;   Mohammed Olfat4 Author Orcid Image ;   Mohammed Saleh5 Author Orcid Image ;   Sherif Roushdy2 Author Orcid Image ;   Yahia Aktham2 Author Orcid Image
Article Authors Cited by (3) Tweetations (2) Metrics

Journals

  1. Alsharhan H, Haider M, Qadoura B, Ayed M, Dhaunsi G, Alkandari H. Enzymatic testing for mucopolysaccharidosis type I in Kuwaiti newborns: a preliminary study toward newborn screening. Frontiers in Pediatrics 2024;12 View
  2. Ramarajan M, Parthasarathy K, Gaikwad K, Joshi N, Garapati K, Kandasamy R, Sharma J, Pandey A. Alterations in Hurler–Scheie Syndrome Revealed by Mass Spectrometry-Based Proteomics and Phosphoproteomics Analysis. OMICS: A Journal of Integrative Biology 2024;28(11):548 View
  3. Johnson G, Gool R, Gaskin K, Wong J, Upadhyay J, Vogel A. Disruptions in speech, language and social communication in lysosomal storage diseases. Neuroscience & Biobehavioral Reviews 2026;190:106931 View