Paper · 5637795

Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.

Jackson CE and 1 other. Pediatrics, 1968. Cited by 68 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease. Papers, record 5637795. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/5637795

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.; PubMed
Journal: Pediatrics; PubMed
Year: 1968; PubMed
Publication types: Journal Article; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/5637795/; PubMed
The journal: https://conductscience.org/library/journal-index/0376422; PubMed
Citations, by iCite: 68; iCite
Revised in PubMed: 2004-11-17; PubMed

Authors2

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename	Kind	ORCID iD
1	Jackson CE	C E
2	Strehler DA	D A

Source PubMed

Topics22

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
Muscular Dystrophies	Major topic
Pelvis	Major topic
Shoulder	Major topic
Adolescent
Adult
Aged
Aspartate Aminotransferases
Biopsy
Child
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Consanguinity
Creatine Kinase
Facial Muscles
Female
Humans
Male
Middle Aged
Muscles
Pedigree
Sex Factors

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References0

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

None in this release.

Cited by12

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 68 citations.

PMID	Title	Journal	Year	In Papers	Source
40,549,548	Sarcospan protects against LGMD R5 via remodeling of the sarcoglycan complex composition in dystrophic mice.	J Clin Invest	2025	https://conductscience.org/library/papers/40549548	PubMed
9,973,293	Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.	Am J Hum Genet	1999	https://conductscience.org/library/papers/9973293	PubMed
9,246,005	DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene.	Am J Hum Genet	1997	https://conductscience.org/library/papers/9246005	PubMed
8,556,875	Limb girdle muscular dystrophy: a radiologic and manometric study of the pharynx and esophagus.	Dysphagia	1996	https://conductscience.org/library/papers/8556875	PubMed
8,533,766	Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.	Am J Hum Genet	1995	https://conductscience.org/library/papers/8533766	PubMed
7,762,565	Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.	Am J Hum Genet	1995	https://conductscience.org/library/papers/7762565	PubMed
5,714,527	Consanguinity and blood group distribution in an Amish Isolate.	Am J Hum Genet	1968	https://conductscience.org/library/papers/5714527	PubMed
5,699,892	Fortuitous detection of a sporadic carrier of Duchenne's muscular dystrophy.	Humangenetik	1968	https://conductscience.org/library/papers/5699892	PubMed
5,516,239	Amish albinism: a distinctive autosomal recessive phenotype.	Am J Hum Genet	1970	https://conductscience.org/library/papers/5516239	PubMed
2,568,091	Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.	Am J Hum Genet	1989	https://conductscience.org/library/papers/2568091	PubMed

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Genes0

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

None in this release.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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