| scholarly article | Q13442814 |
| P50 | author | Emmanuel Mignot | Q5373255 |
| Marcelo A. Fernández-Viña | Q59750308 | ||
| P2093 | author name string | Nicole Fabien | |
| Jérôme Honnorat | |||
| Véronique Rogemond | |||
| Aude Belbezier | |||
| Bastien Joubert | |||
| Gonzalo Montero-Martin | |||
| P2860 | cites work | Autoantibodies to glutamic acid decarboxylase in patients with therapy-resistant epilepsy | Q73986186 |
| Familial case reports of stiff-person syndrome | Q87186429 | ||
| Associations between HLA class II alleles in a North Indian population | Q28280332 | ||
| Familial neuromyelitis optica. | Q34054970 | ||
| Stiff Person syndrome and other anti-GAD-associated neurologic disorders | Q34344939 | ||
| Disease-specific monoclonal antibodies targeting glutamate decarboxylase impair GABAergic neurotransmission and affect motor learning and behavioral functions | Q34471519 | ||
| GAD Antibody-Associated Late-Onset Cerebellar Ataxia in Two Female Siblings | Q34792143 | ||
| Antibodies to inhibitory synaptic proteins in neurological syndromes associated with glutamic acid decarboxylase autoimmunity. | Q35182392 | ||
| Presence of anti-GAD in a non-diabetic population of adults; time dynamics and clinical influence: results from the HUNT study | Q35802307 | ||
| High-throughput, high-fidelity HLA genotyping with deep sequencing | Q36001436 | ||
| Shared Genetic Basis for Type 1 Diabetes, Islet Autoantibodies, and Autoantibodies Associated With Other Immune-Mediated Diseases in Families With Type 1 Diabetes | Q36092713 | ||
| Higher autoantibody levels and recognition of a linear NH2-terminal epitope in the autoantigen GAD65, distinguish stiff-man syndrome from insulin-dependent diabetes mellitus. | Q36363509 | ||
| Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency | Q37378028 | ||
| Diagnostic value of CSF findings in antibody-associated limbic and anti-NMDAR-encephalitis. | Q38073975 | ||
| Novel monogenic diseases causing human autoimmunity | Q38564442 | ||
| Autoantibodies to GABA-ergic neurons and pancreatic beta cells in stiff-man syndrome | Q41196484 | ||
| Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter | Q44898767 | ||
| Is neuromyelitis optica associated with human leukocyte antigen? | Q44965114 | ||
| Potential role of anti-GAD antibodies in abnormal eye movements | Q46435062 | ||
| HLA-DQ association and allele competition in Chinese narcolepsy | Q46990379 | ||
| High GAD65 autoantibody levels in nondiabetic adults are associated with HLA but not with CTLA-4 or INS VNTR. | Q48017173 | ||
| Effects of anti-glutamic acid decarboxylase antibodies associated with neurological diseases | Q48122020 | ||
| Prevalence and immunological spectrum of temporal lobe epilepsy with glutamic acid decarboxylase antibodies. | Q48726404 | ||
| Seroprevalence of autoantibodies against brain antigens in health and disease | Q48774317 | ||
| Cerebellar ataxia with anti-glutamic acid decarboxylase antibodies: study of 14 patients | Q49029367 | ||
| Six-locus high resolution HLA haplotype frequencies derived from mixed-resolution DNA typing for the entire US donor registry. | Q51193836 | ||
| Spectrum of neurological syndromes associated with glutamic acid decarboxylase antibodies: diagnostic clues for this association. | Q51689887 | ||
| Humoral and Cellular Autoimmune Responses in Stiff Person Syndrome | Q52956428 | ||
| Genetics of susceptibility and resistance to insulin-dependent diabetes in stiff-man syndrome. | Q54193067 | ||
| Characteristics of in-vitro phenotypes of glutamic acid decarboxylase 65 autoantibodies in high-titre individuals | Q57148226 | ||
| Comparison of HLA class II alleles in Gypsy and Czech populations by DNA typing with oligonucleotide probes | Q68143916 | ||
| Association of HLA-DQB1*0201 with stiff-man syndrome | Q72662228 | ||
| P433 | issue | 1 | |
| P304 | page(s) | e416 | |
| P577 | publication date | 2017-12-05 | |
| P1433 | published in | Neurology(R) neuroimmunology & neuroinflammation | Q27725776 |
| P1476 | title | Multiplex family with GAD65-Abs neurologic syndromes | |
| P478 | volume | 5 |
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