Cargando…

Assessment of Bone Mineral Status in Children With Marfan Syndrome

Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder with skeletal involvement. It is caused by mutations in fibrillin1 (FBN1) gene resulting in activation of TGF-β, which developmentally regulates bone mass and matrix properties. There is no consensus regarding bone mineralizat...

Descripción completa

Detalles Bibliográficos
Autores principales:	Grover, Monica, Brunetti-Pierri, Nicola, Belmont, John, Phan, Kelly, Tran, Alyssa, Shypailo, Roman J, Ellis, Kenneth J, Lee, Brendan H
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wiley Subscription Services, Inc., A Wiley Company 2012
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429634/ https://www.ncbi.nlm.nih.gov/pubmed/22887731 http://dx.doi.org/10.1002/ajmg.a.35540

Ejemplares similares

The Effect of Cardiorespiratory Fitness and Insulin Resistance on Bone Health in Hispanic Children
por: Shawar, Reem S, et al.
Publicado: (2021)

Infiltrating giant cell tumor in a case of Paget’s disease of bone
por: Nuzzo, Vincenzo, et al.
Publicado: (2009)

Ventricular‐Vascular Coupling in Marfan and Non‐Marfan Aortopathies
por: Loeper, Farina, et al.
Publicado: (2016)

Gene therapy for inborn errors of liver metabolism: progress towards clinical applications
por: Brunetti-Pierri, Nicola
Publicado: (2008)

Liver gene therapy: The magic bullet for the sick lung
por: Brunetti-Pierri, Nicola
Publicado: (2022)

Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome
por: Stagi, Stefano, et al.
Publicado: (2016)

Marfan's Syndrome
por: Bhatia, Tanuj, et al.
Publicado: (2012)

Marfan on the Move
por: de Waard, Vivian
Publicado: (2017)

Marfan Syndrome
por: Sivasankari, T, et al.
Publicado: (2017)

New Screening Tool for Aortic Root Dilation in Children with Marfan Syndrome and Marfan-Like Disorders
por: Wozniak-Mielczarek, Lidia, et al.
Publicado: (2020)

A cross‐sectional study on fatigue, anxiety, and symptoms of depression and their relation with medical status in adult patients with Marfan syndrome. Psychological consequences in Marfan syndrome
por: van Andel, Mitzi M., et al.
Publicado: (2022)

Echocardiographic findings in children with Marfan syndrome
por: Ozdemir, Osman, et al.
Publicado: (2011)

Bone Mineral Status in Children with Epilepsy: Biochemical and Radiologic Markers
por: Hasaneen, Bothina, et al.
Publicado: (2017)

Phenylbutyrate increases activity of pyruvate dehydrogenase complex
por: Ferriero, Rosa, et al.
Publicado: (2013)

Challenges and Prospects for Helper-Dependent Adenoviral Vector-Mediated Gene Therapy
por: Piccolo, Pasquale, et al.
Publicado: (2014)

Liver CHOP‐and‐change stress response
por: Piccolo, Pasquale, et al.
Publicado: (2022)

A retrograde approach for liver gene transfer
por: Brunetti-Pierri, Nicola, et al.
Publicado: (2022)

Influence of weight status on bone mineral content measured by DXA in children
por: Ferrer, Francisco Sánchez, et al.
Publicado: (2021)

Assessment of the Nutritional Status, Bone Mineralization, and Anthropometrics of Children with Thalassemia Major
por: BULGURCU, Serap Cevher, et al.
Publicado: (2021)

Endovascular Repair of Aortic Dissection in Marfan Syndrome: Current Status and Future Perspectives
por: Parisi, Rosario, et al.
Publicado: (2015)

Evaluation of Bone Mineral Status in Adolescent Idiopathic Scoliosis
por: Pourabbas Tahvildari, Babak, et al.
Publicado: (2014)

Primary midgut volvulus in a patient with Marfan syndrome
por: Guragain, Richesh, et al.
Publicado: (2019)

Intraocular Lens Subluxation in Marfan Syndrome
por: Rodrigo, Bolaños-Jiménez, et al.
Publicado: (2014)

Marfan syndrome: current perspectives
por: Pepe, Guglielmina, et al.
Publicado: (2016)

Marfan syndrome: An eyesight of syndrome()
por: Kumar, Ashok, et al.
Publicado: (2014)

The Prevalence of Marfan Syndrome in Korea
por: Jang, Shin Yi, et al.
Publicado: (2017)

Cardiovascular manifestations in Marfan syndrome
por: Lazea, Cecilia, et al.
Publicado: (2021)

The Molecular Genetics of Marfan Syndrome
por: Du, Qiu, et al.
Publicado: (2021)

A retrospective analysis of bone mineral status in patients requiring spinal surgery
por: Schmidt, Tobias, et al.
Publicado: (2018)

Epigenetic control of vascular smooth muscle cells in Marfan and non-Marfan thoracic aortic aneurysms
por: Gomez, Delphine, et al.
Publicado: (2011)

Differences in Cardiovascular Manifestation of Marfan Syndrome Between Children and Adults
por: Wozniak-Mielczarek, L., et al.
Publicado: (2018)

Autophagy master regulator TFEB induces clearance of toxic SERPINA1/α-1-antitrypsin polymers
por: Pastore, Nunzia, et al.
Publicado: (2013)

Visual outcome and surgical results in children with Marfan syndrome
por: Rezar‐Dreindl, Sandra, et al.
Publicado: (2019)

Thrombolysis in a stroke patient with Marfan syndrome
por: Chembala, J, et al.
Publicado: (2012)

Analysis of GPR126 polymorphisms and their relationship with scoliosis in Marfan syndrome and Marfan-like syndrome in Mexican patients
por: Soto, Maria Elena, et al.
Publicado: (2023)

Genome-wide methylation patterns in Marfan syndrome
por: van Andel, Mitzi M., et al.
Publicado: (2021)

Body composition and bone mineral status in patients with Turner syndrome
por: Shi, Kun, et al.
Publicado: (2016)

Ensuring continuity of care for children with inherited metabolic diseases at the time of COVID-19: the experience of a metabolic unit in Italy
por: Brunetti-Pierri, Nicola, et al.
Publicado: (2020)

Biometric and structural ocular manifestations of Marfan syndrome
por: Gehle, Petra, et al.
Publicado: (2017)

Vitamin D Insufficiency and Bone Mineral Status in a Population of Newcomer Children in Canada
por: Vatanparast, Hassanali, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_2aqv38fp68hl845pluib8oau64