Posts Tagged: Christelle Tesson

Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology. HUMAN GENETICS 2015 (REVIEW), Tesson, Koht & Stevanin

Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology. HUMAN GENETICS 2015 (REVIEW), Tesson, Koht & Stevanin Christelle Tesson, Jeanette Koht, Giovanni Stevanin http://link.springer.com/article/10.1007/s00439-015-1536-7 Abstract Hereditary spastic paraplegias (HSP) are rare

Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology. HUMAN GENETICS 2015 (REVIEW), Tesson, Koht & Stevanin

Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology. HUMAN GENETICS 2015 (REVIEW), Tesson, Koht & Stevanin Christelle Tesson, Jeanette Koht, Giovanni Stevanin http://link.springer.com/article/10.1007/s00439-015-1536-7 Abstract Hereditary spastic paraplegias (HSP) are rare

Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion. JNNP 2014

J Neurol Neurosurg Psychiatry. 2014 Dec 4 online Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion. Obayashi M, Stevanin G, Synofzik M, Monin ML, Duyckaerts C, Sato N, Streichenberger

Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion. JNNP 2014

J Neurol Neurosurg Psychiatry. 2014 Dec 4 online Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion. Obayashi M, Stevanin G, Synofzik M, Monin ML, Duyckaerts C, Sato N, Streichenberger

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Ecole Pratique des Hautes Etudes annual seminars, Paris, April 8

Spastic paraplegias SPG28 and SPG49 as examples of human hereditary diseases at the Ecole Pratique des Hautes Etudes annual seminars, Paris, April 8, by Christelle Tesson. Program-2013

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Ecole Pratique des Hautes Etudes annual seminars, Paris, April 8

Spastic paraplegias SPG28 and SPG49 as examples of human hereditary diseases at the Ecole Pratique des Hautes Etudes annual seminars, Paris, April 8, by Christelle Tesson. Program-2013

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Abstract Hereditary spastic paraplegia (HSP) is considered one of the most heterogeneous groups of neurological disorders, both clinically and genetically. The disease comprises pure and complex forms that clinically include slowly progressive lower-limb spasticity resulting from degeneration of the corticospinal

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Abstract Hereditary spastic paraplegia (HSP) is considered one of the most heterogeneous groups of neurological disorders, both clinically and genetically. The disease comprises pure and complex forms that clinically include slowly progressive lower-limb spasticity resulting from degeneration of the corticospinal