Florian Eichler, MD

Neurology Massachusetts General Hospital, Boston, MA 
ALD, HSAN1, Tay Sachs
"Florian Eichler"
Mean distance: 16.01 (cluster 6)
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Jun BK, Chandra A, Kuljis D, et al. (2015) Substrate Availability of Mutant SPT Alters Neuronal Branching and Growth Cone Dynamics in Dorsal Root Ganglia. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 13713-9
Musolino PL, Gong Y, Snyder JM, et al. (2015) Brain endothelial dysfunction in cerebral adrenoleukodystrophy. Brain : a Journal of Neurology
Helman G, Van Haren K, Bonkowsky JL, et al. (2015) Disease specific therapies in leukodystrophies and leukoencephalopathies. Molecular Genetics and Metabolism. 114: 527-36
Vanderver A, Prust M, Tonduti D, et al. (2015) Case definition and classification of leukodystrophies and leukoencephalopathies. Molecular Genetics and Metabolism. 114: 494-500
Gong Y, Mu D, Prabhakar S, et al. (2015) Adenoassociated virus serotype 9-mediated gene therapy for x-linked adrenoleukodystrophy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 23: 824-34
Fridman V, Oaklander AL, David WS, et al. (2015) Natural history and biomarkers in hereditary sensory neuropathy type 1. Muscle & Nerve. 51: 489-95
Krishnamoorthy KS, Eichler F, Rapalino O, et al. (2014) Case records of the Massachusetts General Hospital. Case 14-2014. An 11-month-old girl with developmental delay. The New England Journal of Medicine. 370: 1830-41
Musolino PL, Lund TC, Pan J, et al. (2014) Hematopoietic stem cell transplantation in the leukodystrophies: a systematic review of the literature. Neuropediatrics. 45: 169-74
Berger J, Forss-Petter S, Eichler FS. (2014) Pathophysiology of X-linked adrenoleukodystrophy Biochimie. 98: 135-142
Eichler FS. (2014) Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease: Fifth Edition. 331-336
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