Clinical and Genetic Study of Friedreich’s Ataxia and Ataxia with Vitamin E Deficiency in 44 Moroccan Families. Fatima Imounan, Naima Bouslam, El Hachmia Aitbenhaddou1, Wafa Regragui1, Ahmed Bouhouche, Ali Benomar, Mohammed Yahyaoui; World Journal of Neuroscience, 2014, 4, 299-305, Published Online August 2014 in SciRes. http://www.scirp.org/journal/wjns
http://dx.doi.org/10.4236/wjns.2014.44033
Friday, July 25, 2014
Autosomal Recessive Cerebellar Ataxias
Autosomal Recessive Cerebellar Ataxias; Dr. Anne Noreau, Dr. Nicolas Dupré, Dr. Jean-Pierre Bouchard, Dr. Patrick A. Dion, Dr. Guy A. Rouleau; Handbook of the Cerebellum and Cerebellar Disorders, 2013, pp 2177-2191
FULL TEXT PDF
FULL TEXT PDF
Prise en charge pluridisciplinaire des déformations du tronc chez l’enfant et l’adolescent polyhandicapé
Prise en charge pluridisciplinaire des déformations du tronc chez l’enfant et l’adolescent polyhandicapé; R. Vialle, A. Dubory, H. Bouloussa, P. Mary, S. Zakine; Archives de Pédiatrie, Volume 21, Issue 5, Supplement 1, May 2014, Pages 149-150, ISSN 0929-693X, http://dx.doi.org/10.1016/S0929-693X(14)71505-2.
Prévalence des scolioses dans l'Ataxie de Friedreich 80%. L’amélioration des techniques chirurgicales, mais d’abord et avant tout réanimatoires, pneumologiques, cardiologiques et anesthésiques, permet de proposer des solutions chirurgicales plus ou moins complexes à un très grand nombre de patients, y compris les plus fragiles.
Prévalence des scolioses dans l'Ataxie de Friedreich 80%. L’amélioration des techniques chirurgicales, mais d’abord et avant tout réanimatoires, pneumologiques, cardiologiques et anesthésiques, permet de proposer des solutions chirurgicales plus ou moins complexes à un très grand nombre de patients, y compris les plus fragiles.
Thursday, July 24, 2014
New results ease previous concerns that gene-editing techniques could add unwanted mutations to stem cells
New results ease previous concerns that gene-editing techniques could add unwanted mutations to stem cells. Medicalnewstoday, Sunday 13 July 2014
The iPSC could be much more than a tool for research, wait and see ...
The researcher says: "doesn't necessarily mean that there are no inherent risks to using stem cells with edited genes, but that the editing process doesn't make the stem cells any less safe."
The iPSC could be much more than a tool for research, wait and see ...
The researcher says: "doesn't necessarily mean that there are no inherent risks to using stem cells with edited genes, but that the editing process doesn't make the stem cells any less safe."
AVANCES EN EL TRATAMIENTO DE LAS ATAXIAS CRÓNICAS-Therapeutic developments in chronic ataxias
AVANCES EN EL TRATAMIENTO DE LAS ATAXIAS CRÓNICAS-Therapeutic developments in chronic ataxias. Buompadre MC.; Medicina (B Aires). 2013;73 Suppl 1:49-54.
Palabras clave: ataxia cerebelosa, tratamiento, agentes antioxidantes, corticoides, vitamina
KEYWORDS: antioxidant agents; cerebellar ataxia; corticosteroid; treatment; vitamin
[Article in Spanish]
FREE FULL TEXT PDF
Palabras clave: ataxia cerebelosa, tratamiento, agentes antioxidantes, corticoides, vitamina
KEYWORDS: antioxidant agents; cerebellar ataxia; corticosteroid; treatment; vitamin
[Article in Spanish]
FREE FULL TEXT PDF
Wednesday, July 23, 2014
Genes and Genetic Testing in Hereditary Ataxias
Genes and Genetic Testing in Hereditary Ataxias. Sandford, E.; Burmeister, M.; Genes. 2014; 5(3):586-603.
OPEN ACCESS, FULL TEXT PDF
OPEN ACCESS, FULL TEXT PDF
Sunday, July 20, 2014
Therapeutic approaches for the treatment of Friedreich’s ataxia
Therapeutic approaches for the treatment of Friedreich’s ataxia, Cassandra J Strawser, Kimberly A Schadt, David R Lynch, 2014, Ahead of Print : Pages 1-9 (doi: 10.1586/14737175.2014.939173)
Keywords: coenzyme Q10, deferiprone, EPI-743, EPO, Friedreich ataxia, gene therapy, idebenone, mitochondrial dysfunction, tat-frataxin
Keywords: coenzyme Q10, deferiprone, EPI-743, EPO, Friedreich ataxia, gene therapy, idebenone, mitochondrial dysfunction, tat-frataxin
Friday, July 18, 2014
Sleep and sleep disorders in rare hereditary diseases: a reminder for the pediatrician, pediatric and adult neurologist, general practitioner, and sleep specialist
Sleep and sleep disorders in rare hereditary diseases: a reminder for the pediatrician, pediatric and adult neurologist, general practitioner, and sleep specialist. Review article, Natan Gadoth and imageArie Oksenberg, Front. Neurol., 17 July 2014 | doi: 10.3389/fneur.2014.00133
The authors suggest that snoring and obstructive sleep apnea (OSA) in FRDA is related to disease duration and the presence of reduced respiratory muscle strength in conjunction with scoliosis and poor posture.
The authors suggest that snoring and obstructive sleep apnea (OSA) in FRDA is related to disease duration and the presence of reduced respiratory muscle strength in conjunction with scoliosis and poor posture.
Wednesday, July 16, 2014
Sensitivity of Spatiotemporal Gait Parameters in Measuring Disease Severity in Friedreich Ataxia
Sensitivity of Spatiotemporal Gait Parameters in Measuring Disease Severity in Friedreich Ataxia. Sarah C. Milne, Darren R. Hocking, Nellie Georgiou-Karistianis, Anna Murphy, Martin B. Delatycki, Louise A. Corben; The Cerebellum July 2014
Spatiotemporal gait parameters are a sensitive measure of gait decline in individuals with FRDA and should be considered for inclusion in intervention studies whilst participants are still ambulant.
Spatiotemporal gait parameters are a sensitive measure of gait decline in individuals with FRDA and should be considered for inclusion in intervention studies whilst participants are still ambulant.
Coexistence of tuberous sclerosis and Friedreich ataxia
Coexistence of tuberous sclerosis and Friedreich ataxia. Melanie Walker, Ali Samii, Thomas Bird; Journal of the Neurological Sciences Volume 221, Issue 1 , Pages 91-93, 15 June 2004
"The occurrence of two mutations on the same chromosome is probably coincidental but emphasizes the importance of searching for additional genetic causes when the phenotype does not fit with an established genetic diagnosis."
"The occurrence of two mutations on the same chromosome is probably coincidental but emphasizes the importance of searching for additional genetic causes when the phenotype does not fit with an established genetic diagnosis."
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