Friday, April 4, 2014

Friedreich’s Ataxia: From Molecular Biology to the Quest for Therapies

Friedreich’s Ataxia: From Molecular Biology to the Quest for Therapies;

Lecture abstract

Genetics of hereditary neurological disorders in children

Genetics of hereditary neurological disorders in children. Yue Huang, Sui Yu, Zhanhe Wu, Beisha Tang; Translational Pediatrics, Vol 3, No 2 (April 2014); doi: 10.3978/j.issn.2224-4336.2014.03.04

Review Article

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Frataxin Silencing Inactivates Mitochondrial Complex I in NSC34 Motoneuronal Cells and Alters Glutathione Homeostasis

Frataxin Silencing Inactivates Mitochondrial Complex I in NSC34 Motoneuronal Cells and Alters Glutathione Homeostasis. Carletti, B.; Piermarini, E.; Tozzi, G.; Travaglini, L.; Torraco, A.; Pastore, A.; Sparaco, M.; Petrillo, S.; Carrozzo, R.; Bertini, E.; Piemonte, F; International Journal of Molecular Sciences. 2014; 15(4):5789-5806.

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A 7 year old girl with hypertrophic cardiomyopathy and progressive scoliosis

A 7 year old girl with hypertrophic cardiomyopathy and progressive scoliosis. Radhika Dhamija, Salman Kirmani; Seminars in Pediatric Neurology, Available online 3 April 2014, ISSN 1071-9091, http://dx.doi.org/10.1016/j.spen.2014.04.003.

Wednesday, April 2, 2014

Friedreich’s Ataxia: FDA Orphan Drug Designations

Friedreich’s Ataxia: FDA Orphan Drug Designations. The Orphan Druganaut Blog, March 25, 2014

Chart which identifies all FDA Orphan Drug Designations (ODDs) for FRDA in ascending date order

The role of frataxin in doxorubicin-mediated cardiac hypertrophy

The role of frataxin in doxorubicin-mediated cardiac hypertrophy . Shravanthi Mouli, Gayani Nanayakkara, Rain Fu, Avery Berlin, Abdul Alasmari, Robert Arnold and Rajesh Amin; The FASEB Journal vol. 28 no. 1 Supplement 648.6, April 2014

Keywords: Heart failure, cancer chemotherapeutic, doxorubicin (DOX), cardiac hypertrophy, Frataxin (FXN)

Sunday, March 30, 2014

Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration

Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration. Nicole I. Wolf, Michel Koenig; Handbook of Clinical Neurology, Volume 113, 2013, Pages 1869–1878; Pediatric Neurology Part III. http://dx.doi.org/10.1016/B978-0-444-59565-2.00057-5

The hereditary ataxias with onset in childhood are a group of heterogeneous disorders, usually with autosomal recessive inheritance. In many of them, magnetic resonance imaging (MRI) shows cerebellar atrophy. The most prominent exception to this is Friedreich's ataxia, where MRI shows normal cerebellar volume, but sometimes spinal cord atrophy.

Friday, March 28, 2014

HEART FAILURE BURDEN IN CHILDREN AND ADULTS WITH FRIEDREICH ATAXIA

HEART FAILURE BURDEN IN CHILDREN AND ADULTS WITH FRIEDREICH ATAXIA . Carol Wittlieb-Weber, Joseph Rossano, David Lynch, Kimberly Lin; Journal of the American College of Cardiology, Volume 63, Issue 12, Supplement, 1 April 2014, Pages A835; http://dx.doi.org/10.1016/S0735-1097(14)60835-4

"Attention to the degree of cardiac involvement is critical in the management of patients with FA."