Discover Community Create You

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

An unusual pathologic feature and phenotype associated with familial hyperkalemic periodic paralysis.

European journal of neurology - 1 Jun 2008

Kang Sa-Yoon, Kim Joong-Seok, Choi Jae Chol, Kang Ji-Hoon, Lee Jung Seok

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Creatine Kinase
Share to Electromyography
Share to Muscle, Skeletal
Share to Myositis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to NAV1.4 Voltage-Gated Sodium Channel

Share to Pedigree

Share to Phenotype

Share to Sodium Channels

Source

Identifiers

PMID: 18410368
DOI: 10.1111/j.1468-1331.2008.02135.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

An unusual pathologic feature and phenotype associated with familial hyperkalemic periodic paralysis.PMID 18410368Read ↗

An atypical CaV1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis.Semantic proximity Read ↗

A Novel CLCN1 Gene Mutation Associated with Hypokalemic Periodic Paralysis in a Pregnant Woman.Semantic proximity Read ↗

Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder.Semantic proximity Read ↗

Primary Periodic Paralyses: A Review of Etiologies and Their PathogenesesSemantic proximity Read ↗

Diverse phenotype of hypokalaemic periodic paralysis within a family.Semantic proximity Read ↗

Tumor necrosis factor receptor-associated periodic syndrome in a pediatric patient: A genetic diagnosis.Semantic proximity Read ↗

[Familial hypokalemic periodic paralysis].Semantic proximity Read ↗

An expanding view for the molecular basis of familial periodic paralysis.Semantic proximity Read ↗

Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis.Semantic proximity Read ↗

A new clinical entity in T704M mutation in periodic paralysis.Semantic proximity Read ↗

Thyrotoxic Hypokalemic Periodic Paralysis: Pathophysiological Mechanisms.Semantic proximity Read ↗

Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause?Semantic proximity Read ↗

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