List of works by Jill S Goldman

17q-linked frontotemporal dementia-amyotrophic lateral sclerosis without tau mutations with tau and alpha-synuclein inclusions

scientific article published in March 2004

A qualitative study of the impact of a dementia experiential learning project on pre-medical students: a friend for Rachel

scientific article published on 02 May 2019

Amyotrophic lateral sclerosis and spinocerebellar ataxia type 2 in a family with full CAG repeat expansions of ATXN2.

scientific article

Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint

scientific article published on 01 January 2020

Case Report: Depression vs. Early-Onset Alzheimer Disease: The Genetic Counselor's Role

scientific article published in October 2001

Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration

scientific article published on 06 January 2020

Comparison of family histories in FTLD subtypes and related tauopathies

scientific article

Early-onset Alzheimer disease: when is genetic testing appropriate?

scientific article published in April 2004

Ethical Issues in Cancer Genetics: 1) Whose Information Is It?

article

Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors

scientific article published in June 2011

Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion

scientific article

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

scientific article published on 01 January 2020

Genetic testing and counseling in the diagnosis and management of young-onset dementias.

scientific article published on 18 March 2015

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

scientific article published on 06 January 2020

Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72.

scientific article

Multiple system atrophy and repeat expansions in C9orf72--reply.

scientific article published on September 2014

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

scientific article

New approaches to genetic counseling and testing for Alzheimer's disease and frontotemporal degeneration

scientific article

Predictive testing for neurodegenerative diseases in the age of next-generation sequencing

scientific article published on 08 October 2020

Psychiatric symptoms in preclinical behavioural-variant frontotemporal dementia in MAPT mutation carriers.

scientific article published on 20 January 2018

Pure hereditary spastic paraplegia due to a de novo mutation in the NIPA1 gene

scientific article published on 10 December 2013

Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort

scientific article published on 13 July 2020

Screening for C9ORF72 repeat expansion in FTLD.

scientific article published on 27 March 2012

The Confluence of Psychiatric Symptoms and Neurodegenerative Disease: Impact on Genetic Counseling.

scientific article published on 24 December 2016

Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriers

scientific article published on 15 August 2019

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

scientific article published on 01 January 2020

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