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Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy

Neurology, 2003-08, Vol.61 (3), p.369-374

2003

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Adrenoleukodystrophy : phenotype, genetics, pathogenesis and therapy

Brain (London, England : 1878), 1997-08, Vol.120 (8), p.1485-1508

MOSER, H. W

1997

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Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls

Annals of neurology, 1999-01, Vol.45 (1), p.100-110

1999

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Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophy

Neurology, 2002-03, Vol.58 (6), p.901-907

2002

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Increase of pollinator attraction by means of a visual signal in the sexually deceptive orchid, Ophrys heldreichii (Orchidaceae)

Plant systematics and evolution, 2007-03, Vol.264 (1/2), p.31-40

2007

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PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts

Journal of inherited metabolic disease, 2009-02, Vol.32 (1), p.109-119

2009

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MRI and proton MRSI in women heterozygous for X-linked adrenoleukodystrophy

Neurology, 2003-04, Vol.60 (8), p.1301-1307

2003

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Mutations in the PTS1 receptor gene, PXR1 , define complementation group 2 of the peroxisome biogenesis disorders

Nature genetics, 1995-02, Vol.9 (2), p.115-125

1995

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Adrenomyeloneuropathy: A Neuropathologic Review Featuring Its Noninflammatory Myelopathy

Journal of neuropathology and experimental neurology, 2000-02, Vol.59 (2), p.89-102

2000

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X-Linked adrenoleukodystrophy: overview and prognosis as a function of age and brain magnetic resonance imaging abnormality. A study involving 372 patients

Neuropediatrics, 2000-10, Vol.31 (5), p.227

2000

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Magnetization transfer MRI demonstrates spinal cord abnormalities in adrenomyeloneuropathy

Neurology, 2005-05, Vol.64 (10), p.1739-1745

2005

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Diffusion tensor brain MR imaging in X-linked cerebral adrenoleukodystrophy

Neurology, 2001-02, Vol.56 (4), p.544-547

2001

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Neuroimaging studies in Rett syndrome

Brain & development (Tokyo. 1979), 2001-12, Vol.23, p.S62-S71

2001

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Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

Nature genetics, 1997-12, Vol.17 (4), p.445-448

1997

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Spectroscopic evidence of cerebral axonopathy in patients with "pure" adrenomyeloneuropathy

Neurology, 2005-01, Vol.64 (2), p.304-310

2005

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Dendritic Anomalies in Disorders Associated with Mental Retardation

Cerebral cortex (New York, N.Y. 1991), 2000-10, Vol.10 (10), p.981-991

2000

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Peroxisomal Bifunctional Protein Deficiency Revisited: Resolution of Its True Enzymatic and Molecular Basis

American journal of human genetics, 1999, Vol.64 (1), p.99-107

1999

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Bone marrow transplantation for infantile ceramidase deficiency (Farber disease)

Bone marrow transplantation (Basingstoke), 2000-08, Vol.26 (3), p.357-363

2000

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Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening

Annals of neurology, 2001-04, Vol.49 (4), p.512-517

2001

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Identification of PEX10, the Gene Defective in Complementation Group 7 of the Peroxisome-Biogenesis Disorders

American journal of human genetics, 1998-08, Vol.63 (2), p.347-359

1998

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The Inflammatory Myelinopathy of Adreno-Leukodystrophy: Cells, Effector Molecules, and Pathogenetic Implications

Journal of neuropathology and experimental neurology, 1992-11, Vol.51 (6), p.630-643

1992

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Plasma and red blood cell fatty acids in peroxisomal disorders

Neurochemical research, 1999-02, Vol.24 (2), p.187-197

1999

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X-linked Adrenoleukodystrophy: The Role of Contrast-enhanced MR Imaging in Predicting Disease Progression

American journal of neuroradiology : AJNR, 2000-05, Vol.21 (5), p.839-844

2000

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Adrenoleukodystrophy: Phenotypic variability and implications for therapy

Journal of inherited metabolic disease, 1992-01, Vol.15 (4), p.645-664

1992

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MR findings in adult-onset adrenoleukodystrophy

American journal of neuroradiology : AJNR, 1995-06, Vol.16 (6), p.1227-1237

1995

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Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy

Adrenoleukodystrophy : phenotype, genetics, pathogenesis and therapy

Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls

Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophy

Increase of pollinator attraction by means of a visual signal in the sexually deceptive orchid, Ophrys heldreichii (Orchidaceae)

PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts

MRI and proton MRSI in women heterozygous for X-linked adrenoleukodystrophy

Mutations in the PTS1 receptor gene, PXR1 , define complementation group 2 of the peroxisome biogenesis disorders

Adrenomyeloneuropathy: A Neuropathologic Review Featuring Its Noninflammatory Myelopathy

X-Linked adrenoleukodystrophy: overview and prognosis as a function of age and brain magnetic resonance imaging abnormality. A study involving 372 patients

Magnetization transfer MRI demonstrates spinal cord abnormalities in adrenomyeloneuropathy

Diffusion tensor brain MR imaging in X-linked cerebral adrenoleukodystrophy

Neuroimaging studies in Rett syndrome

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

Spectroscopic evidence of cerebral axonopathy in patients with "pure" adrenomyeloneuropathy

Dendritic Anomalies in Disorders Associated with Mental Retardation

Peroxisomal Bifunctional Protein Deficiency Revisited: Resolution of Its True Enzymatic and Molecular Basis

Bone marrow transplantation for infantile ceramidase deficiency (Farber disease)

Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening

Identification of PEX10, the Gene Defective in Complementation Group 7 of the Peroxisome-Biogenesis Disorders

The Inflammatory Myelinopathy of Adreno-Leukodystrophy: Cells, Effector Molecules, and Pathogenetic Implications

Plasma and red blood cell fatty acids in peroxisomal disorders

X-linked Adrenoleukodystrophy: The Role of Contrast-enhanced MR Imaging in Predicting Disease Progression

Adrenoleukodystrophy: Phenotypic variability and implications for therapy

MR findings in adult-onset adrenoleukodystrophy

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