Cargando…

Cardiac magnetic resonance imaging in Alström syndrome

BACKGROUND: A case series of the cardiac magnetic resonance imaging findings in seven adult Alström patients. METHODS: Seven patients from the National Specialist Commissioning Group Centre for Alström Disease, Torbay, England, UK, completed the cardiac magnetic resonance imaging protocol to assess...

Descripción completa

Detalles Bibliográficos
Autores principales:	Loudon, Margaret A, Bellenger, Nicholas G, Carey, Catherine M, Paisey, Richard B
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2009
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2705344/ https://www.ncbi.nlm.nih.gov/pubmed/19515241 http://dx.doi.org/10.1186/1750-1172-4-14

Ejemplares similares

Heterogeneity and causation of organ dysfunction in Alström syndrome
por: Paisey, R, et al.
Publicado: (2012)

Duration of Diabetes Predicts Aortic Pulse Wave Velocity and Vascular Events in Alström Syndrome
por: Paisey, Richard B., et al.
Publicado: (2015)

Alström syndrome: a paradigm for diffuse fibrosis and clinical progression
por: Edwards, Nicola C, et al.
Publicado: (2013)

Refining genotype–phenotype correlation in Alström syndrome through study of primary human fibroblasts
por: Chen, Jian‐Hua, et al.
Publicado: (2017)

Cellular modelling of Alström syndrome in human primary dermal fibroblasts and derived cells
por: Semple, RK, et al.
Publicado: (2012)

Prospective cardiovascular magnetic resonance imaging in adults with Alström syndrome: silent progression of diffuse interstitial fibrosis
por: Baig, Shanat, et al.
Publicado: (2020)

Protection From Clinical Peripheral Sensory Neuropathy in Alström Syndrome in Contrast to Early-Onset Type 2 Diabetes
por: Paisey, Richard B., et al.
Publicado: (2009)

Consensus clinical management guidelines for Alström syndrome
por: Tahani, Natascia, et al.
Publicado: (2020)

Diffuse left ventricular interstitial fibrosis is associated with sub-clinical myocardial dysfunction in Alström Syndrome: an observational study
por: Edwards, Nicola C., et al.
Publicado: (2015)

Brain involvement in Alström syndrome
por: Citton, Valentina, et al.
Publicado: (2013)

Alström syndrome: current perspectives
por: Álvarez-Satta, María, et al.
Publicado: (2015)

Alström Syndrome: Genetics and Clinical Overview
por: Marshall, Jan D, et al.
Publicado: (2011)

Magnetic Resonance Imaging in Cardiology
por: Bellenger, Nick, et al.
Publicado: (1999)

Bardet-Biedl and Alström syndromes in Spain
por: Valverde, D, et al.
Publicado: (2012)

Alström syndrome caused by maternal uniparental disomy
por: Lopour, Madeline Q.R., et al.
Publicado: (2022)

ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits
por: Hearn, Tom
Publicado: (2018)

Monogenic diabetes syndromes: Locus‐specific databases for Alström, Wolfram, and Thiamine‐responsive megaloblastic anemia
por: Astuti, Dewi, et al.
Publicado: (2017)

Cilia, Alström Syndrome – molecular mechanisms and therapeutic perspectives
por: Cristina, Maria Mihai, et al.
Publicado: (2008)

Alstrom syndrome in four sibs from northern Jordan
por: Hamamy, Hanan, et al.
Publicado: (2006)

Molecular and Phenotypic Expansion of Alström Syndrome in Chinese Patients
por: Zhang, Qianwen, et al.
Publicado: (2022)

Proteomic and Transcriptomic Landscapes of Alström and Bardet–Biedl Syndromes
por: Smyczynska, Urszula, et al.
Publicado: (2022)

A Role for Alström Syndrome Protein, Alms1, in Kidney Ciliogenesis and Cellular Quiescence
por: Li, Guochun, et al.
Publicado: (2007)

Ocular evaluation and genetic test for an early Alström Syndrome diagnosis
por: Etheridge, Tyler, et al.
Publicado: (2020)

Novel ALMS1 mutations in Chinese patients with Alström syndrome
por: Liang, Xiaofang, et al.
Publicado: (2013)

Adipose Tissue Malfunction Drives Metabolic Dysfunction in Alström Syndrome
por: Kang, Sona
Publicado: (2021)

Novel Mutations of the ALMS1 Gene in Patients with Alström Syndrome
por: Wang, Chunmei, et al.
Publicado: (2021)

Alström Syndrome: A Rare Cause of Severe Insulin Resistance
por: Radi, Suhaib, et al.
Publicado: (2022)

Alstrom syndrome (OMIM 203800): a case report and literature review
por: Joy, Tisha, et al.
Publicado: (2007)

Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
por: Marozio, Luca, et al.
Publicado: (2022)

Alström syndrome: A rare association of retinitis pigmentosa with insulin resistance syndrome
por: Wani, Irfan Yousuf, et al.
Publicado: (2013)

Liver Fibrosis and Steatosis in Alström Syndrome: A Genetic Model for Metabolic Syndrome
por: Bettini, Silvia, et al.
Publicado: (2021)

Molecular approach in the study of Alström syndrome: Analysis of ten Spanish families
por: Piñeiro-Gallego, Teresa, et al.
Publicado: (2012)

Alstrom syndrome: A rare genetic disorder and its anaesthetic significance
por: Tiwari, Akhilesh, et al.
Publicado: (2010)

Supportive care in a patient with Alstrom syndrome with hyperphenylalaninemia and sleep problems
por: Jalilolghadr, Shabnam, et al.
Publicado: (2023)

EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome
por: Farmer, Amy, et al.
Publicado: (2013)

Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes
por: Bakar, Ayman A., et al.
Publicado: (2017)

The utility of cardiac magnetic resonance imaging in Kounis syndrome
por: Okur, Aylin, et al.
Publicado: (2015)

Role of cardiac magnetic resonance imaging in troponinemia syndromes
por: Nguyen Nguyen, Nhung, et al.
Publicado: (2022)

Metabolic Syndrome Features Presenting in Early Childhood in Alström Syndrome: A Case Report
por: Pirgon, Özgür, et al.
Publicado: (2009)

Mutations in Alström Protein Impair Terminal Differentiation of Cardiomyocytes
por: Shenje, Lincoln T., et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_pl54sqh5c694vp3eccoi29t5na