Cargando…

Should persons with autosomal dominant AD be included in clinical trials? Authors' response

Detalles Bibliográficos
Autores principales:	Szigeti, Kinga, Doody, Rachelle S
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2011
Materias:	Letter
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226308/ https://www.ncbi.nlm.nih.gov/pubmed/21631907 http://dx.doi.org/10.1186/alzrt81

Ejemplares similares

Should persons with autosomal dominant AD be included in clinical trials?
por: Grill, Joshua D, et al.
Publicado: (2011)

Should EOAD patients be included in clinical trials?
por: Szigeti, Kinga, et al.
Publicado: (2011)

Cerebral Microbleeds in Autosomal Dominant Polycystic Kidney Disease
por: Tsai, Li-Kai, et al.
Publicado: (2020)

Autosomal dominant optic atrophy and cataract “plus” phenotype including axonal neuropathy
por: Horga, Alejandro, et al.
Publicado: (2019)

Should we screen for intracranial aneurysms in children with autosomal dominant polycystic kidney disease?
por: Walker, Emma Y. X., et al.
Publicado: (2022)

Visual and psychological morbidity among patients with autosomal dominant optic atrophy
por: Bailie, Maura, et al.
Publicado: (2013)

A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma
por: Kinsler, VA, et al.
Publicado: (2015)

Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease
por: Cadnapaphornchai, Melissa A.
Publicado: (2017)

Should central venous catheters be used to drain pleural effusions? Authors' response
por: Singh, Kulgit, et al.
Publicado: (2004)

Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity
por: Hadj-Rabia, Smail, et al.
Publicado: (2013)

Mutation-independent gene knock-in therapy targeting 5′UTR for autosomal dominant retinitis pigmentosa
por: Hoang, Duc Anh, et al.
Publicado: (2023)

Hay-Wells syndrome of ectodermal dysplasia: A rare autosomal dominant disorder
por: Nagaveni, N. B., et al.
Publicado: (2011)

Autosomal Dominant Cerebral Small Vessel Disease in HTRA1 Gene Mutation
por: Mahale, Rohan R., et al.
Publicado: (2021)

Response to “Fibroblast Growth Factor 23 Is a Valuable Predictor of Autosomal Dominant Polycystic Kidney Disease Progression”
por: Yu, Alan S.L., et al.
Publicado: (2021)

Sturge–Weber syndrome coexisting with autosomal dominant polycystic kidney disease
por: Niemczyk, Mariusz, et al.
Publicado: (2012)

Autosomal dominant intellectual disability
por: Wieczorek, Dagmar
Publicado: (2018)

Autosomal dominant polycystic kidney
por: Gudadhe, Rugaved Raghavendra, et al.
Publicado: (2022)

Should kidney volume be used as an indicator of surgical occasion for patients with autosomal dominant polycystic kidney disease?
por: Yu, Jiang, et al.
Publicado: (2018)

Autosomal Dominant Alzheimer Disease: A Unique Resource to Study CSF Biomarker Changes in Preclinical AD
por: Schindler, Suzanne Elizabeth, et al.
Publicado: (2015)

Large hemorrhagic ovarian cyst in postmenopausal patient with autosomal dominant polycystic kidney disease
por: Mishra, V. V., et al.
Publicado: (2016)

Erythropoietin and Fibroblast Growth Factor 23 in Autosomal Dominant Polycystic Kidney Disease Patients
por: Hanudel, Mark R., et al.
Publicado: (2019)

CSF1R Related Leukoencephalopathy - Rare Childhood Presentation of An Autosomal Dominant Microgliopathy!
por: Sriram, Neeharika, et al.
Publicado: (2022)

Apelin is altered in subjects with autosomal dominant polycystic kidney disease and preserved kidney function
por: Janssens, Peter, et al.
Publicado: (2023)

High water vs. ad libitum water intake for autosomal dominant polycystic kidney disease: a randomized controlled feasibility trial
por: El-Damanawi, R, et al.
Publicado: (2020)

High water vs. ad libitum water intake for autosomal dominant polycystic kidney disease: a randomized controlled feasibility trial
por: El-Damanawi, R, et al.
Publicado: (2020)

Authors should know the ethical rules of publication
por: Yousef Khan, Fahmi
Publicado: (2010)

Prognostic Enrichment Design in Clinical Trials for Autosomal Dominant Polycystic Kidney Disease
por: Steinman, Theodore
Publicado: (2016)

Neuropsychiatric and sleep study in autosomal dominant dopa-responsive dystonia
por: Alves Júnior, Ailton C., et al.
Publicado: (2022)

A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease
por: Jamshidi, Javad, et al.
Publicado: (2016)

Pathogenic Variant of REEP1 in a Korean Family with Autosomal-Dominant Hereditary Spastic Paraplegia
por: Park, Hyung Jun, et al.
Publicado: (2018)

Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy “in disguise”
por: Grandis, Marina, et al.
Publicado: (2018)

A Rare Case Report of Emphysematous Cyst Infection in Autosomal Dominant Polycystic Kidney Disease
por: Sethi, Jasmine, et al.
Publicado: (2019)

Simultaneous kidney transplantation and ipsilateral native nephrectomy in patients with autosomal dominant polycystic kidney disease
por: Gadelkareem, Rabea Ahmed, et al.
Publicado: (2022)

Radial pseudoaneurysm following coronary angiography in a patient with autosomal dominant polycystic kidney disease
por: Emrich, Insa E., et al.
Publicado: (2023)

Cold temperature improves mobility and survival in Drosophila models of autosomal-dominant hereditary spastic paraplegia (AD-HSP)
por: Baxter, Sally L., et al.
Publicado: (2014)

Zebrafish Models of Autosomal Dominant Ataxias
por: Quelle-Regaldie, Ana, et al.
Publicado: (2021)

Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy
por: Cerino, Mathieu, et al.
Publicado: (2020)

IGF-1 in autosomal dominant cerebellar ataxia - open-label trial
por: Sanz-Gallego, Irene, et al.
Publicado: (2014)

Randomised controlled trial of high versus ad libitum water intake in patients with autosomal dominant polycystic kidney disease: rationale and design of the DRINK feasibility trial
por: El-Damanawi, Ragada, et al.
Publicado: (2018)

Autosomal Dominant Centronuclear Myopathy with Unique Clinical Presentations
por: Lee, Jee-Young, et al.
Publicado: (2007)

Cannot write session to /tmp/vufind_sessions/sess_vpb62ie97gklqgqgfsmclbn5qt