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504 Development and pilot test of a palliative care interview guide for children with cystic fibrosis: the ADAPT-Cystic Fibrosis

Journal of cystic fibrosis, 2023-10, Vol.22, p.S266-S267

2023

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P246 Improving assessment of palliative care needs among cystic fibrosis children: a Delphi study of the ADAPT-Cystic Fibrosis communication guide

Journal of cystic fibrosis, 2022-06, Vol.21, p.S135

2022

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432 Illness burden in adults with CF is associated with sex, race, ethnicity, and social risk factors

Journal of cystic fibrosis, 2024-09, Vol.23, p.S231-S232

2024

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409 Exploring cystic fibrosis providers’ perceptions of palliative care performance: baseline data from the Improving Life with Cystic Fibrosis multisite implementation trial for primary palliative care intervention

Journal of cystic fibrosis, 2023-10, Vol.22, p.S211-S212

2023

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EPS2.10 Initial validation of the Integrated Palliative Care Outcome Scale (IPOS) in adults with cystic fibrosis (CF): data from the Improving Life with CF multicentre pragmatic implementation trial

Journal of cystic fibrosis, 2023-06, Vol.22, p.S42-S43

2023

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411 The Improving Life with Cystic Fibrosis multisite implementation trial for primary palliative care intervention in U.S. cystic fibrosis centers: initial uptake and feasibility data

Journal of cystic fibrosis, 2023-10, Vol.22, p.S213-S213

2023

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219: Improving assessment for CF pediatric palliative care: Initial development of the ADAPT-CF communication guide with children and caregivers

Journal of cystic fibrosis, 2021-11, Vol.20, p.S107

2021

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223: Development of a CF primary palliative care intervention: Perceptions and preferences of individuals with CF and family caregivers

Journal of cystic fibrosis, 2021-11, Vol.20, p.S109

2021

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242 Palliative care needs in cystic fibrosis: Baseline data from the Improving Life with Cystic Fibrosis Multi-site Implementation Trial for Primary Palliative Care Intervention

Journal of cystic fibrosis, 2022-10, Vol.21, p.S143-S144

2022

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P254 Development of a primary palliative care model that includes a novel approach to address the needs of caregivers of adults with cystic fibrosis - improving life with cystic fibrosis: a primary palliative care partnership

Journal of cystic fibrosis, 2021, Vol.20, p.S116-S117

2021

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An early start to Huntington's disease

Science (American Association for the Advancement of Science), 2020-08, Vol.369 (6505), p.771-772

DiFiglia, Marian

2020

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Huntingtin-lowering strategies in Huntington's disease: Antisense oligonucleotides, small RNAs, and gene editing

Movement disorders, 2014-09, Vol.29 (11), p.1455-1461

2014

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Cortisone in polyostotic fibrous dysplasia

New York State journal of medicine, 1951-11, Vol.51 (22), p.2665

DI FIGLIA, S E

1951

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ACTH and morphine addiction in bronchial asthma

New York State journal of medicine, 1952-02, Vol.52 (4), p.474

DI FIGILIA, S E

1952

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Allele-selective lowering of mutant HTT protein by HTT–LC3 linker compounds

Nature (London), 2019-11, Vol.575 (7781), p.203-209

2019

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The recycling endosome and its role in neurological disorders

Progress in neurobiology, 2012-05, Vol.97 (2), p.127-141

2012

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Therapeutic Silencing of Mutant Huntingtin with siRNA Attenuates Striatal and Cortical Neuropathology and Behavioral Deficits

Proceedings of the National Academy of Sciences - PNAS, 2007-10, Vol.104 (43), p.17204-17209

2007

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A toxic mutant huntingtin species is resistant to selective autophagy

Nature chemical biology, 2017-11, Vol.13 (11), p.1152-1154

2017

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Optimized Cholesterol-siRNA Chemistry Improves Productive Loading onto Extracellular Vesicles

Molecular therapy, 2018-08, Vol.26 (8), p.1973-1982

2018

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Protein changes in synaptosomes of Huntington's disease knock-in mice are dependent on age and brain region

Neurobiology of disease, 2020-07, Vol.141, p.104950-104950, Article 104950

2020

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Altered Parvalbumin-Positive Neuron Distribution in Basal Ganglia of Individuals with Tourette Syndrome

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (37), p.13307-13312

2005

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Early whole-body mutant huntingtin lowering averts changes in proteins and lipids important for synapse function and white matter maintenance in the LacQ140 mouse model

Neurobiology of disease, 2023-10, Vol.187, p.106313-106313, Article 106313

2023

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Autophagy and Its Possible Roles in Nervous System Diseases, Damage and Repair

Autophagy, 2005-04, Vol.1 (1), p.11-22

2005

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KEAP1-modifying small molecule reveals muted NRF2 signaling responses in neural stem cells from Huntington’s disease patients

Proceedings of the National Academy of Sciences - PNAS, 2017-06, Vol.114 (23), p.E4676-E4685

2017

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504 Development and pilot test of a palliative care interview guide for children with cystic fibrosis: the ADAPT-Cystic Fibrosis

P246 Improving assessment of palliative care needs among cystic fibrosis children: a Delphi study of the ADAPT-Cystic Fibrosis communication guide

432 Illness burden in adults with CF is associated with sex, race, ethnicity, and social risk factors

409 Exploring cystic fibrosis providers’ perceptions of palliative care performance: baseline data from the Improving Life with Cystic Fibrosis multisite implementation trial for primary palliative care intervention

EPS2.10 Initial validation of the Integrated Palliative Care Outcome Scale (IPOS) in adults with cystic fibrosis (CF): data from the Improving Life with CF multicentre pragmatic implementation trial

411 The Improving Life with Cystic Fibrosis multisite implementation trial for primary palliative care intervention in U.S. cystic fibrosis centers: initial uptake and feasibility data

219: Improving assessment for CF pediatric palliative care: Initial development of the ADAPT-CF communication guide with children and caregivers

223: Development of a CF primary palliative care intervention: Perceptions and preferences of individuals with CF and family caregivers

242 Palliative care needs in cystic fibrosis: Baseline data from the Improving Life with Cystic Fibrosis Multi-site Implementation Trial for Primary Palliative Care Intervention

P254 Development of a primary palliative care model that includes a novel approach to address the needs of caregivers of adults with cystic fibrosis - improving life with cystic fibrosis: a primary palliative care partnership

An early start to Huntington's disease

Huntingtin-lowering strategies in Huntington's disease: Antisense oligonucleotides, small RNAs, and gene editing

Cortisone in polyostotic fibrous dysplasia

ACTH and morphine addiction in bronchial asthma

Allele-selective lowering of mutant HTT protein by HTT–LC3 linker compounds

The recycling endosome and its role in neurological disorders

Therapeutic Silencing of Mutant Huntingtin with siRNA Attenuates Striatal and Cortical Neuropathology and Behavioral Deficits

A toxic mutant huntingtin species is resistant to selective autophagy

A divalent siRNA chemical scaffold for potent and sustained modulation of gene expression throughout the central nervous system

Optimized Cholesterol-siRNA Chemistry Improves Productive Loading onto Extracellular Vesicles

Protein changes in synaptosomes of Huntington's disease knock-in mice are dependent on age and brain region

Altered Parvalbumin-Positive Neuron Distribution in Basal Ganglia of Individuals with Tourette Syndrome

Early whole-body mutant huntingtin lowering averts changes in proteins and lipids important for synapse function and white matter maintenance in the LacQ140 mouse model

Autophagy and Its Possible Roles in Nervous System Diseases, Damage and Repair

KEAP1-modifying small molecule reveals muted NRF2 signaling responses in neural stem cells from Huntington’s disease patients

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