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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Goizet, C; Boukhris, A; Maltete, D; Guyant-Maréchal, L; Truchetto, J; Mundwiller, E; Hanein, S; Jonveaux, P; Roelens, F; Loureiro, J; Godet, E; Forlani, S; Melki, J; Auer-Grumbach, M; Fernandez, JC; Martin-Hardy, P; Sibon, I; Sole, G; Orignac, I; Mhiri, C; Coutinho, P; Durr, A; Brice, A; Stevanin, G.
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.
Neurology. 2009; 73(14): 1111-1119. Doi: 10.1212/WNL.0b013e3181bacf59
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Auer-Grumbach Michaela
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Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Brain - pathology
Carrier Proteins - genetics
Child -
Corpus Callosum - pathology
Female -
Humans -
Magnetic Resonance Imaging -
Male -
Mutation -
Positron-Emission Tomography - methods
Severity of Illness Index -
Spastic Paraplegia, Hereditary - genetics
Tomography, Emission-Computed, Single-Photon - methods

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