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A Second Family with Autosomal Dominant Burning Feet Syndrome.
- Published in:
- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 445, doi. 10.1111/j.1749-6632.1999.tb08606.x
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- Publication type:
- Article
Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and Results.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 389, doi. 10.1111/j.1749-6632.1999.tb08600.x
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- Publication type:
- Article
Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular Genetics.
- Published in:
- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 60, doi. 10.1111/j.1749-6632.1999.tb08568.x
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- Publication type:
- Article
Hereditary Neuralgic Amyotrophy: Mutation Analysis of Candidate Genes.
- Published in:
- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 443, doi. 10.1111/j.1749-6632.1999.tb08605.x
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- Publication type:
- Article
Preimplantation Diagnosis for Charcot-Marie-Tooth Type 1A.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 460, doi. 10.1111/j.1749-6632.1999.tb08610.x
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- Publication type:
- Article
Mutation Screening of Charcot-Marie-Tooth Patients in Poland.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 493, doi. 10.1111/j.1749-6632.1999.tb08619.x
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- Publication type:
- Article
Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA).
- Published in:
- Human Genetics, 2001, v. 108, n. 5, p. 390, doi. 10.1007/s004390100510
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- Publication type:
- Article
Cholesterol and triglycerides moderate the effect of apolipoprotein E on memory functioning in older adults.
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- 2007
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- Publication type:
- Journal Article
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.
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- Pflügers Archiv: European Journal of Physiology, 2000, v. 439, n. 7, p. r208, doi. 10.1007/BF03376574
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- Publication type:
- Article
Peripheral myelin protein-22 expression in charcot-marie-tooth disease type 1a sural nerve biopsies.
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- Journal of Neuroscience Research, 1994, v. 37, n. 5, p. 654, doi. 10.1002/jnr.490370513
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- Publication type:
- Article
Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family.
- Published in:
- 2004
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- Publication type:
- Letter
Electronic EJHG: The Web and the Wider World.
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- European Journal of Human Genetics, 2004, v. 12, n. 1, p. 1, doi. 10.1038/sj.ejhg.5201139
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- Publication type:
- Article
Phosphatidylinositol 2-kinase activity is required for the expression of glial fibrillary acidic protein upon camp-dependent induction of differentiation in rat C6 glioma
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- Journal of Neurochemistry, 2001, v. 76, n. 2, p. 610, doi. 10.1046/j.1471-4159.2001.00077.x
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- Publication type:
- Article
Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A.
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- Molecular Human Reproduction, 1998, v. 4, n. 10, doi. 10.1093/molehr/4.10.978
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- Publication type:
- Article
Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.
- Published in:
- Annals of Human Genetics, 2001, v. 65, n. 6, p. 517, doi. 10.1017/S0003480001008910
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- Publication type:
- Article
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A (CMT1A) using molecular genetic techniques.
- Published in:
- 1995
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- Publication type:
- journal article
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families.
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- Nature, 1987, v. 329, n. 6135, p. 153, doi. 10.1038/329153a0
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- Publication type:
- Article
Sexual dimorphism in the dermal armour of cordyline lizards (Squamata: Cordylinae).
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- Biological Journal of the Linnean Society, 2018, v. 125, n. 5, p. 30, doi. 10.1093/biolinnean/bly096
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- Publication type:
- Article
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites.
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- Molecular Psychiatry, 2012, v. 17, n. 2, p. 223, doi. 10.1038/mp.2011.24
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- Publication type:
- Article
Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families.
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- Molecular Psychiatry, 2008, v. 13, n. 4, p. 442, doi. 10.1038/sj.mp.4002039
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- Publication type:
- Article
HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study.
- Published in:
- 2007
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- Publication type:
- Letter
A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression.
- Published in:
- Molecular Psychiatry, 2004, v. 9, n. 3, p. 287, doi. 10.1038/sj.mp.4001420
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- Publication type:
- Article
Genetics of personality: are we making progress?
- Published in:
- Molecular Psychiatry, 2003, v. 8, n. 10, p. 840, doi. 10.1038/sj.mp.4001367
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- Publication type:
- Article
A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorder.
- Published in:
- Molecular Psychiatry, 2003, v. 8, n. 1, p. 83, doi. 10.1038/sj.mp.4001190
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- Publication type:
- Article
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.
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- Molecular Psychiatry, 2002, v. 7, n. 10, p. 1064, doi. 10.1038/sj.mp.4001198
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- Publication type:
- Article
Epistatic effect of genes from the dopamine and serotonin systems on the temperament traits of Novelty Seeking and Harm Avoidance.
- Published in:
- Molecular Psychiatry, 2002, v. 7, n. 5, p. 448, doi. 10.1038/sj.mp.4001005
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- Publication type:
- Article
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxia.
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- Molecular Psychiatry, 2000, v. 5, n. 4, p. 439, doi. 10.1038/sj.mp.4000747
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- Publication type:
- Article
High-level transgene expression in primary human T lymphocytes and adult bone marrow CD34<sup>+</sup> cells via electroporation-mediated gene delivery.
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- Gene Therapy, 2000, v. 7, n. 16, p. 1431, doi. 10.1038/sj.gt.3301252
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- Publication type:
- Article
Nonviral transfection of distinct types of human dendritic cells: high-efficiency gene transfer by electroporation into hematopoietic progenitor- but not monocyte-derived dendritic cells.
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- Gene Therapy, 1998, v. 5, n. 5, p. 700, doi. 10.1038/sj.gt.3300626
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- Publication type:
- Article
Apolipoprotein E epsilon4 and the risk of dementia with stroke. A population-based investigation.
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- 1997
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- Publication type:
- journal article
TARDBP mutation p. Ile383 Val associated with semantic dementia and complex proteinopathy.
- Published in:
- Neuropathology & Applied Neurobiology, 2014, v. 40, n. 2, p. 225, doi. 10.1111/nan.12063
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- Publication type:
- Article
Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7).
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- Neuropathology & Applied Neurobiology, 2008, v. 34, n. 5, p. 479, doi. 10.1111/j.1365-2990.2007.00933.x
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- Publication type:
- Article
Spinocerebellar ataxia type 7 (SCA7): widespread brain damage in an adult-onset patient with progressive visual impairments in comparison with an adult-onset patient without visual impairments.
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- Neuropathology & Applied Neurobiology, 2008, v. 34, n. 2, p. 155, doi. 10.1111/j.1365-2990.2007.00882.x
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- Publication type:
- Article
Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7.
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- Neuropathology & Applied Neurobiology, 2006, v. 32, n. 6, p. 635, doi. 10.1111/j.1365-2990.2006.00772.x
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- Publication type:
- Article
mRNA-electroporated mature dendritic cells retain transgene expression, phenotypical properties and stimulatory capacity after cryopreservation.
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- Leukemia (08876924), 2002, v. 16, n. 7, p. 1324, doi. 10.1038/sj.leu.2402511
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- Publication type:
- Article
Gene-based cancer vaccines: an ex vivo approach.
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- Leukemia (08876924), 2001, v. 15, n. 4, p. 545, doi. 10.1038/sj.leu.2402069
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- Publication type:
- Article
Gene therapy: principles and applications to hematopoietic cells.
- Published in:
- 2001
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- Publication type:
- journal article
Lack of association between GABRA3 and unipolar affective disorder: a multicentre study.
- Published in:
- International Journal of Neuropsychopharmacology, 2001, v. 4, n. 3, p. 273, doi. 10.1017/S1461145701002449
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- Publication type:
- Article
Hereditary neuralgic amyotrophy (HNA) is genetically heterogeneous.
- Published in:
- 2002
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- Publication type:
- Abstract
A CLONE CONTIG OF 12Q24.3 ENCOMPASSING THE DISTAL HEREDITARY MOTOR NEUROPATHY TYPE II GENE.
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- Journal of the Peripheral Nervous System, 2000, v. 5, n. 4, p. 242, doi. 10.1111/j.1529-8027.2000.22-25.x
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- Publication type:
- Article
Fabry disease in a patient with Turner syndrome.
- Published in:
- 2009
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- Publication type:
- Report
Granulin mutations associated with frontotemporal lobar degeneration and related disorders: An update.
- Published in:
- 2008
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- Publication type:
- Other
Progranulin locus deletion in frontotemporal dementia.
- Published in:
- Human Mutation, 2008, v. 29, n. 1, p. 53, doi. 10.1002/humu.20651
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- Publication type:
- Article
Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragment.
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- Human Mutation, 2006, v. 27, n. 9, p. 888, doi. 10.1002/humu.20402
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- Publication type:
- Article
The role of tau ( MAPT) in frontotemporal dementia and related tauopathies.
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- Human Mutation, 2004, v. 24, n. 4, p. 277, doi. 10.1002/humu.20086
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- Publication type:
- Article
Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe(Communicated by Richard G.H. Cotton).
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- Human Mutation, 2003, v. 22, n. 5, p. 409, doi. 10.1002/humu.10269
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- Publication type:
- Article
The Association between APOE Genotype and Memory Dysfunction in Subjects with Mild Cognitive Impairment Is Related to Age and Alzheimer Pathology.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2008, v. 26, n. 2, p. 101, doi. 10.1159/000144072
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- Publication type:
- Article
Positive Association between the GABRA5 Gene and Unipolar Recurrent Major Depression.
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- Neuropsychobiology, 1997, v. 36, n. 2, p. 62, doi. 10.1159/000119363
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- Publication type:
- Article
Manic-Depressive Illness and Linkage Reanalysis in the Xq27-Xq28 Region of Chromosome X.
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- Neuropsychobiology, 1995, v. 31, n. 2, p. 58, doi. 10.1159/000119173
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- Publication type:
- Article
Influence of diet on prehension mode in cordylid lizards: a morphological and kinematic analysis.
- Published in:
- Journal of Zoology, 2013, v. 291, n. 4, p. 286, doi. 10.1111/jzo.12075
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- Publication type:
- Article