H. Moser

发表

Neuronal migration abnormality in peroxisomal bifunctional enzyme defect

H. Moser, A. Moser, W. Kaufmann, 1996, Annals of neurology.

Peroxisomal Disorders: Overview

A. Moser, H. Moser, 1996, Annals of the New York Academy of Sciences.

Linkage of adrenoleukodystrophy to a polymorphic DNA probe

D. Meyers, P. Aubourg, G. Sack, 1987, Annals of neurology.

A new dietary therapy for adrenoleukodystrophy: Biochemical and preliminary clinical results in 36 patients

A. Moser, D. Sanders, D. Cornblath, 1987, Annals of neurology.

Lorenzo oil therapy for adrenoleukodystrophy: A prematurely amplified hope

H. Moser, 1993, Annals of neurology.

Adrenoleukodystrophy: From Bedside to Molecular Biology

H. Moser, 1987, Journal of child neurology.

Cataplexy in variant forms of Niemann‐Pick disease

H. Singer, R. Kandt, Hugo W. Moser, 1982, Annals of neurology.

Genetic peroxisomal disorders: Why, when, and how to test

G. Raymond, H. Moser, 1998, Annals of neurology.

Neuroanatomy of Rett syndrome: A volumetric imaging study

A. Reiss, R. Bryan, M. Abrams, 1993, Annals of neurology.

Imaging cortical association tracts in the human brain using diffusion‐tensor‐based axonal tracking

H. Moser, G. Pearlson, C. Davatzikos, 2002, Magnetic resonance in medicine.

Neurological and neuropathologic heterogeneity in two brothers with cobalamin C deficiency

J. T. Black, A. Moser, R. Schmidt, 2001, Annals of neurology.

Visual system abnormalities in adrenomyeloneuropathy

R. Tusa, P. Kaplan, B. Kruse, 1995, Annals of neurology.

Cerebral X‐linked adrenoleukodystrophy in a girl with Xq27‐Ter deletion

H. Moser, A. Moser, G. Narkis, 2002, Annals of neurology.

Pathogenetic mechanisms in peroxisomal disorders

H. Moser, 1996, Current Opinion in Neurology.

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

H. Moser, A. Moser, G. Raymond, 2001, Annals of neurology.

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

H. Moser, E. Melhem, G. Raymond, 2003, Neurology.

X-linked adrenoleukodystrophy: the role of contrast-enhanced MR imaging in predicting disease progression.

H. Moser, E. Melhem, G. Raymond, 2000, AJNR. American journal of neuroradiology.

Adrenoleukodystrophy: a scoring method for brain MR observations.

H. Moser, A. Stillman, R. Latchaw, 1994, AJNR. American journal of neuroradiology.

MR findings in adult-onset adrenoleukodystrophy.

A. J. Kumar, H. Moser, A. Bergin, 1995, AJNR. American journal of neuroradiology.

Follow-up of 89 asymptomatic patients with adrenoleukodystrophy treated with Lorenzo's oil.

H. Moser, A. Moser, E. Melhem, 2005, Archives of neurology.

Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy.

H. Moser, H W Moser, H. Moser, 1997, Brain : a journal of neurology.

Localized proton magnetic resonance spectroscopy in patients with adult adrenoleukodystrophy. Increase of choline compounds in normal appearing white matter.

H. Moser, N. Baumann, E. Cabanis, 1997, Archives of neurology.

Childhood cerebral form of adrenoleukodystrophy: short-term effect of bone marrow transplantation on brain MR observations.

H. Moser, A. Stillman, R. Latchaw, 1994, AJNR. American journal of neuroradiology.

Long-term effect of bone-marrow transplantation for childhood-onset cerebral X-linked adrenoleukodystrophy

I. Jambaqué, C. Cox, S. Blanche, 2000, The Lancet.

Ocular clinicopathologic correlation of Hallervorden-Spatz syndrome with acanthocytosis and pigmentary retinopathy.

H. Moser, W. Green, A. Clark, 1983, American journal of ophthalmology-glaucoma.

Dendritic anomalies in disorders associated with mental retardation.

H. Moser, W. Kaufmann, H. Moser, 1999, Cerebral cortex.

CSF findings in adrenoleukodystrophy: correlation between measures of cytokines, IgG production, and disease severity.

H. Moser, B. Blazar, J. Phillips, 1994, Pediatric neurology.

Adrenoleukodystrophy: Phenotypic variability and implications for therapy

H. Moser, A. Moser, J. Ott, 1992, Journal of Inherited Metabolic Disease.

Clinical aspects of adrenoleukodystrophy and adrenomyeloneuropathy.

H. Moser, A. Moser, A. Bergin, 1991, Developmental neuroscience.

Lorenzo's oil and thrombocytopenia in patients with adrenoleukodystrophy.

W. Zinkham, J. Borel, T. Kickler, 1993, The New England journal of medicine.

Childhood adrenoleukodystrophy. Failure of intensive immunosuppression to arrest neurologic progression.

H. Moser, D. Griffin, M. Bresnan, 1988, Archives of neurology.

Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.

H. Moser, D. Valle, S. Gould, 1998, American journal of human genetics.

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

H. Moser, F. Eichler, G. Raymond, 2002, Neurology.

Peroxisomal Disorders: Genotype, Phenotype, Major Neuropathologic Lesions, and Pathogenesis

H. Moser, J. Powers, H. Moser, 1998 .

Adrenoleukodystrophy: Biochemical procedures in diagnosis, prevention and treatment

H. Moser, P. Watkins, S. Naidu, 1987, Journal of Inherited Metabolic Disease.

Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome

H. Moser, A. Moser, R. Kelley, 2004, Acta Neuropathologica.

Rett syndrome--natural history in 70 cases.

H. Moser, J. Opitz, S. Naidu, 1986, American journal of medical genetics. Supplement.

Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomes.

H. Moser, A. Moser, A. Das, 1992, The Journal of biological chemistry.

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

H. Moser, A. Moser, L. Nagae-Poetscher, 2003, Neurology.

Nerve conduction studies in adrenomyeloneuropathy.

H. Moser, D. Cornblath, V. Chaudhry, 1996, Journal of neurology, neurosurgery, and psychiatry.

Argininosuccinic aciduria: Report of two new cases and demonstration of intermittent elevation of blood ammonia

H. Moser, C. Neumann, M. L. Efron, 1967 .

Neonatal seizures and retardation in a girl with biochemical features of X‐linked adrenoleukodystrophy

H. Moser, A. Moser, T. Hashimoto, 1988, Neurology.

“Lorenzo’s Oil” Therapy for X-linked Adrenoleukodystrophy: Rationale and Current Assessment of Efficacy

H. Moser, A. Moser, G. Raymond, 2007, Journal of Molecular Neuroscience.

Diffusion tensor–based imaging reveals occult abnormalities in adrenomyeloneuropathy

H. Moser, S. Wakana, L. Nagae-Poetscher, 2005, Annals of neurology.

Spectroscopic evidence of cerebral axonopathy in patients with “pure” adrenomyeloneuropathy

H. Moser, A. Bastian, G. Raymond, 2005, Neurology.

Fetal cerebrohepatorenal (Zellweger) syndrome: dysmorphic, radiologic, biochemical, and pathologic findings in four affected fetuses.

H. Moser, A. Moser, J. Frías, 1985, Human pathology.