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Longer titles found: Familial hemiplegic migraine (view), Sporadic hemiplegic migraine (view)

searching for Hemiplegic migraine 13 found (46 total)

Wartenberg's sign (668 words) [view diff] exact match in snippet view article find links to article

disorders of the cerebral cortex such as mild hemiplegic stroke or hemiplegic migraine where the same clinical finding has been called the "digiti quinti

Lucid interval (540 words) [view diff] exact match in snippet view article find links to article

CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine". Annals of Neurology. 49 (6): 753–760. doi:10.1002/ana.1031. PMID 11409427

SAMM50 (451 words) [view diff] case mismatch in snippet view article find links to article

disease phenotype of Ezra, 9 year old male with Epilepsy, ESES, Hemiplegic Migraine, Exocrine Pancreatic Insuffiency, CSID, Global Apraxia, developmental

PRKCSH (954 words) [view diff] exact match in snippet view article find links to article

Hofker MH, Haan J, Ferrari MD (1997). "A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene.

GNG2 (1,092 words) [view diff] exact match in snippet view article find links to article

PMID 12486123. Melliti K, Grabner M, Seabrook GR (2003). "The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type

Anne Joutel (778 words) [view diff] exact match in snippet view article find links to article

Labauge, H Chabriat, A Nibbio, et al. 1993. A gene for familial hemiplegic migraine maps to chromosome 19. Nature genetics 5 (1), 40-45 (440 citations)

Aura (symptom) (1,768 words) [view diff] case mismatch in snippet view article

Anil; Samanta, Debopam; Emmady, Prabhu D.; Arora, Rohan (2021), "Hemiplegic Migraine", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30020674

List of diseases (H) (1,717 words) [view diff] exact match in snippet view article

Hemihypertrophy intestinal web corneal opacity Hemimegalencephaly Hemiplegia Hemiplegic migraine, familial Hemochromatosis Hemochromatosis type 1 Hemochromatosis

SCN1A (2,607 words) [view diff] case mismatch in snippet view article find links to article

PMID 11823106. S2CID 25555020. GeneReviews/NCBI/NIH/UW entry on Familial Hemiplegic Migraine GeneReviews/NCBI/NIH/UW entry on SCN1A-Related Seizure Disorders

Abdominal migraine (3,106 words) [view diff] exact match in snippet view article find links to article

heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine". Developmental Medicine & Child Neurology. 54 (10). Wiley: 958–960

Sodium channel (5,597 words) [view diff] exact match in snippet view article find links to article

tonic-clonic seizures (ICEGTC), Panayiotopoulos syndrome, familial hemiplegic migraine (FHM), familial autism, Rasmussens's encephalitis and Lennox-Gastaut

Voltage-gated sodium channel (3,587 words) [view diff] exact match in snippet view article find links to article

tonic-clonic seizures (ICEGTC), Panayiotopoulos syndrome, familial hemiplegic migraine (FHM), familial autism, Rasmussens's encephalitis and Lennox-Gastaut

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

cyclic; 162800; ELANE Hematuria, benign familial; 141200; COL4A3 Hemiplegic migraine, familial; 141500; CACNA1A Hemochromatosis, type 2A; 602390; HJV