adrenoleukodystrophy - Page 1

Neuroradiology: Key Differential Diagnoses and Clinical Questions E-Book

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Neuroradiology: Key Differential Diagnoses and Clinical Questions E-Book

Pamela W. Schaefer, Juan E. Small

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Neuroradiology: Key Differential Diagnoses and Clinical Questions E-Book

Pamela W. Schaefer, Juan E. Small

698 pages

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Imaging of the Brain E-Book

Thomas P. Naidich, Mauricio Castillo, Soonmee Cha, James G. Smirniotopoulos

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Imaging of the Brain E-Book

Thomas P. Naidich, Mauricio Castillo, Soonmee Cha, James G. Smirniotopoulos

1984 pages

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Practical Surgical Neuropathology: A Diagnostic Approach E-Book

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Practical Surgical Neuropathology: A Diagnostic Approach E-Book

Arie Perry, Daniel J. Brat

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Practical Surgical Neuropathology: A Diagnostic Approach E-Book

Arie Perry, Daniel J. Brat

987 pages

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Swaiman's Pediatric Neurology - E-Book

Kenneth F. Swaiman, Stephen Ashwal, Donna M Ferriero, Nina F Schor

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Swaiman's Pediatric Neurology - E-Book

Kenneth F. Swaiman, Stephen Ashwal, Donna M Ferriero, Nina F Schor

6339 pages

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Enfermedades peroxisomales. Estado actual

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Enfermedades peroxisomales. Estado actual

R. Palencia

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Autres

Enfermedades peroxisomales. Estado actual

R. Palencia

13 pages

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Chitotriosidase as a biomarker of cerebral adrenoleukodystrophy

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Chitotriosidase as a biomarker of cerebral adrenoleukodystrophy

Orchard, Lund Troy, Miller Wes, Rothman, Raymond Gerald, Nascene David, Basso Lisa, Cloyd James, Tolar, Tolar Jakub

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Chitotriosidase as a biomarker of cerebral adrenoleukodystrophy

Orchard, Lund Troy, Miller Wes, Rothman, Raymond Gerald, Nascene David, Basso Lisa, Cloyd James, Tolar, Tolar Jakub

9 pages

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Preferential expression of mutant ABCD1allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms

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Preferential expression of mutant ABCD1allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms

Salsano Ettore, Tabano Silvia, Sirchia, Colapietro Patrizia, Castellotti Barbara, Gellera Cinzia, Rimoldi Marco, Pensato Viviana, Mariotti Caterina, Pareyson Davide, Miozzo Monica, Uziel Graziella

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Savoirs

Preferential expression of mutant ABCD1allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms

Salsano Ettore, Tabano Silvia, Sirchia, Colapietro Patrizia, Castellotti Barbara, Gellera Cinzia, Rimoldi Marco, Pensato Viviana, Mariotti Caterina, Pareyson Davide, Miozzo Monica, Uziel Graziella

9 pages

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