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Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation

Annals of neurology, 2003-08, Vol.54 (2), p.271-274

2003

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SOS genes are rapidly induced while translesion synthesis polymerase activity is temporally regulated

Frontiers in microbiology, 2024, Vol.15, p.1373344-1373344

2024

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Activation of multiple stress responses in Staphylococcus aureus substantially lowers the minimal inhibitory concentration when combining two novel antibiotic drug candidates

Frontiers in microbiology, 2023-09, Vol.14, p.1260120-1260120

2023

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SCA2 may present as levodopa-responsive parkinsonism

Movement disorders, 2003-04, Vol.18 (4), p.425-429

2003

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Halogenated Pyrrolopyrimidines with Low MIC on Staphylococcus aureus and Synergistic Effects with an Antimicrobial Peptide

Antibiotics (Basel), 2022-07, Vol.11 (8), p.984

2022

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Ageism among health care providers and interventions to improve their attitudes toward older adults: an integrative review

Journal of gerontological nursing, 2012-05, Vol.38 (5), p.26

2012

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Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features

Journal of neurology, 2004-11, Vol.251 (11), p.1398-1401

2004

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Genetic counseling in industry settings: Opportunities in the era of precision health

American journal of medical genetics. Part C, Seminars in medical genetics, 2018-03, Vol.178 (1), p.46-53

2018

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Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature

American journal of medical genetics. Part A, 2018-11, Vol.176 (11), p.2259-2275

2018

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Informed Choice in Direct-to-Consumer Genetic Testing (DTCGT) Websites: A Content Analysis of Benefits, Risks, and Limitations

Journal of genetic counseling, 2012-06, Vol.21 (3), p.433-439

2012

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Halogenated Pyrrolopyrimidines with Low MIC on IStaphylococcus aureus/I and Synergistic Effects with an Antimicrobial Peptide

Antibiotics (Basel), 2022-07, Vol.11 (8)

2022

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Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred)

Movement disorders, 2011-09, Vol.26 (11), p.2134-2136

2011

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Association between cardiac denervation and parkinsonism caused by α‐synuclein gene triplication

Brain (London, England : 1878), 2004-04, Vol.127 (4), p.768-772

2004

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Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2)

Movement disorders, 2004-06, Vol.19 (6), p.622-629

2004

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Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

Neuroscience letters, 2005-07, Vol.382 (1), p.191-194

2005

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Primary hyperhidrosis--evidence for autosomal dominant inheritance

Clinical autonomic research, 2003-04, Vol.13 (2), p.96-98

2003

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Exercise-induced dystonia as a preceding symptom of familial Parkinson's disease

Movement disorders, 2004-02, Vol.19 (2), p.228-230

2004

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Smell testing is abnormal in ‘lubag’ or X-linked dystonia-parkinsonism: a pilot study

Parkinsonism & related disorders, 2004-10, Vol.10 (7), p.407-410

2004

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Familial Lewy Body Diseases

Journal of geriatric psychiatry and neurology, 2002-12, Vol.15 (4), p.217-223

2002

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Association between cardiac denervation and parkinsonism caused by [alpha]-synuclein gene triplication

Brain (London, England : 1878), 2004-04, Vol.127 (4), p.768-768

2004

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Mutation at the SCA17 locus is not a common cause of parkinsonism

Parkinsonism & related disorders, 2003-08, Vol.9 (6), p.317-320

2003

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Primary hyperhidrosis

Clinical autonomic research, 2003-04, Vol.13 (2), p.96-98

2003

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When Caring for Mom Interferes With Your Job

AARP the magazine (A edition), 2022-08, Vol.65 (5A), p.35

Singleton, Amanda

2022

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Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred)

Movement disorders : official journal of the Movement Disorder Society, 2011, Vol.26 (11), p.2134-2136

2011

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Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation

SOS genes are rapidly induced while translesion synthesis polymerase activity is temporally regulated

Activation of multiple stress responses in Staphylococcus aureus substantially lowers the minimal inhibitory concentration when combining two novel antibiotic drug candidates

SCA2 may present as levodopa-responsive parkinsonism

Halogenated Pyrrolopyrimidines with Low MIC on Staphylococcus aureus and Synergistic Effects with an Antimicrobial Peptide

Ageism among health care providers and interventions to improve their attitudes toward older adults: an integrative review

Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features

Genetic counseling in industry settings: Opportunities in the era of precision health

Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature

Informed Choice in Direct-to-Consumer Genetic Testing (DTCGT) Websites: A Content Analysis of Benefits, Risks, and Limitations

Halogenated Pyrrolopyrimidines with Low MIC on IStaphylococcus aureus/I and Synergistic Effects with an Antimicrobial Peptide

Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred)

Association between cardiac denervation and parkinsonism caused by α‐synuclein gene triplication

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2)

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

Primary hyperhidrosis--evidence for autosomal dominant inheritance

Exercise-induced dystonia as a preceding symptom of familial Parkinson's disease

Smell testing is abnormal in ‘lubag’ or X-linked dystonia-parkinsonism: a pilot study

Familial Lewy Body Diseases

Association between cardiac denervation and parkinsonism caused by [alpha]-synuclein gene triplication

Mutation at the SCA17 locus is not a common cause of parkinsonism

Primary hyperhidrosis

When Caring for Mom Interferes With Your Job

Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred)

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