Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Alpha-1-antitrypsin phenotypes and associated disease patterns in neurological patients.

Acta neurologica Scandinavica - 1 May 1995

Lolin Y I, Ward A M

Abstract excerpt

INTRODUCTION: Alpha-1-antitrypsin (AAT) deficiency is usually associated with lung or liver disease. It is often detected as a qualitative reduction of the alpha-1 band on the serum protein electrophoretic pattern. MATERIAL AND METHODS: We examined the protein electrophoretic pattern in sera of 22980 unselected consecutive patients with neurological disorders and noted a reduced alpha-1 band in 88. Their...

Topics

Adult
Aged
Cerebrovascular Disorders
Epilepsy, Tonic-Clonic
Female
Gene Frequency
Humans
Male
Middle Aged
Multiple Sclerosis
Neoplasms
Nervous System Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Phenotype

Retrospective Studies

Risk Factors

alpha 1-Antitrypsin

alpha 1-Antitrypsin Deficiency

Source

Identifiers

PMID: 7639071
DOI: 10.1111/j.1600-0404.1995.tb07027.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7639071-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Alpha-1-antitrypsin phenotypes and associated disease patterns in neurological patients.PMID 7639071Read ↗

α1-Antitrypsin phenotypes and associated serum protein concentrations in a large clinical population.Semantic proximity Read ↗

Panniculitis revealing qualitative alpha 1 antitrypsine deficiency (MS variant).Semantic proximity Read ↗

Prevalence of alpha1-antitrypsin phenotypes in patients with IgA nephropathy.Semantic proximity Read ↗

Estimated Prevalence and Number of PiMZ Genotypes of Alpha-1 Antitrypsin in Seventy-Four Countries Worldwide.Semantic proximity Read ↗

Alpha-1 Antitrypsin Levels and Polymorphisms in Interstitial Lung Diseases.Semantic proximity Read ↗

Distribution of alpha(1)-antitrypsin alleles in patients with bronchiectasis.Semantic proximity Read ↗

alpha 1-Antitrypsin (AAT) deficiency and ANCA-positive systemic vasculitis: genetic and clinical implications.Semantic proximity Read ↗

Alpha-1-antitrypsin associated panniculitis: the MS variant.Semantic proximity Read ↗

Immunohistochemical and genetic characterization of the M Cagliari alpha-1-antitrypsin molecule (M-like alpha-1-antitrypsin deficiency).Semantic proximity Read ↗

Alcoholic liver disease and alpha-1-antitrypsin inclusion globules in PiM phenotype. Case report.Semantic proximity Read ↗

[Alpha-2 Macroglobulin Serum Level in Patients with Alpha-1 Antitrypsin Deficiency].Semantic proximity Read ↗

Microheterogeneity of some serum glycoproteins in neurodegenerative diseases.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.