Found: 24
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The Influence of GBA and LRRK2 on Mood Disorders in Parkinson's Disease.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 4, p. 606, doi. 10.1002/mdc3.13722
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- Publication type:
- Article
Genetic Creutzfeldt Jakob disease: Can MRI serve as an early diagnostic biomarker?
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.057783
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- Publication type:
- Article
Low doses of radiation induce systemic production of cytokines: Possible contribution to leukemogenesis.
- Published in:
- International Journal of Cancer, 1993, v. 55, n. 2, p. 269, doi. 10.1002/ijc.2910550217
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- Publication type:
- Article
Inheritance, Mode of Inheritance, and Candidate Genes for Primary Hyperparathyroidism in Keeshonden.
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- Journal of Veterinary Internal Medicine, 2007, v. 21, n. 1, p. 199, doi. 10.1111/j.1939-1676.2007.tb02948.x
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- Publication type:
- Article
Widespread occurrence of antisense transcription in the human genome.
- Published in:
- Nature Biotechnology, 2003, v. 21, n. 4, p. 379, doi. 10.1038/nbt808
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- Publication type:
- Article
Primary Hyperoxaluria in Cats Is Caused by a Mutation in the Feline GRHPR Gene.
- Published in:
- Journal of Heredity, 2009, v. 100, p. S2, doi. 10.1093/jhered/esp038
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- Publication type:
- Article
Photoreceptor Cell Death, Proliferation and Formation of Hybrid Rod/S-Cone Photoreceptors in the Degenerating STK38L Mutant Retina.
- Published in:
- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024074
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- Publication type:
- Article
Metabolic syndrome does not influence the phenotype of LRRK2 and GBA related Parkinson's disease.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66319-9
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- Publication type:
- Article
Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50573-7
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- Publication type:
- Article
Genomic deletion of CNGB3 is identical by descent in multiple canine breeds and causes achromatopsia.
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- BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-27
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- Publication type:
- Article
Biochemical markers for severity and risk in GBA and LRRK2 Parkinson's disease.
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- Journal of Neurology, 2021, v. 268, n. 4, p. 1517, doi. 10.1007/s00415-020-10325-4
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- Publication type:
- Article
Validity of the Short Weekly Calendar Planning Activity in patients with Parkinson disease and nonmanifesting LRRK2 and GBA carriers.
- Published in:
- European Journal of Neurology, 2024, v. 31, n. 8, p. 1, doi. 10.1111/ene.16327
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- Publication type:
- Article
Glucocerebrosidase Activity Is Not Associated with Parkinson's Disease Risk or Severity.
- Published in:
- Movement Disorders, 2022, v. 37, n. 3, p. 651, doi. 10.1002/mds.28929
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- Publication type:
- Article
Glucocerebrosidase Activity is not Associated with Parkinson's Disease Risk or Severity.
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- Movement Disorders, 2022, v. 37, n. 1, p. 190, doi. 10.1002/mds.28792
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- Publication type:
- Article
A Possible Modifying Effect of the G2019S Mutation in the LRRK2 Gene on GBA Parkinson's Disease.
- Published in:
- 2020
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- Publication type:
- journal article
COL9A2 and COL9A3 mutations in canine autosomal recessive oculoskeletal dysplasia.
- Published in:
- Mammalian Genome, 2010, v. 21, n. 7/8, p. 398, doi. 10.1007/s00335-010-9276-4
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- Publication type:
- Article
Canine RD3 mutation establishes rod-cone dysplasia type 2 ( rcd2) as ortholog of human and murine rd3.
- Published in:
- Mammalian Genome, 2009, v. 20, n. 2, p. 109, doi. 10.1007/s00335-008-9163-4
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- Publication type:
- Article
R869C mutation in molecular motor KIF17 gene is involved in dementia with Lewy bodies.
- Published in:
- Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2021, v. 13, n. 1, p. 1, doi. 10.1002/dad2.12143
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- Publication type:
- Article
Correction: The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.
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- 2023
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- Publication type:
- Correction Notice
The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.
- Published in:
- BMC Neurology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12883-023-03193-8
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- Publication type:
- Article
The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.
- Published in:
- BMC Neurology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12883-023-03193-8
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- Publication type:
- Article
MAPT Locus in Parkinson's Disease Patients of Ashkenazi Origin: A Stratified Analysis.
- Published in:
- Genes, 2024, v. 15, n. 1, p. 46, doi. 10.3390/genes15010046
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- Publication type:
- Article
C9orf72 -G 4 C 2 Intermediate Repeats and Parkinson's Disease; A Data-Driven Hypothesis.
- Published in:
- Genes, 2021, v. 12, n. 8, p. 1210, doi. 10.3390/genes12081210
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- Publication type:
- Article
X-linked recessive primary retinal dysplasia is linked to the Norrie disease locus.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 8, p. 1295
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- Publication type:
- Article