Anne B. Johnson

发表

F. Barkhof, B. Banwell, Richard Robinson, 2005, Annals of neurology.

Mitochondrial abnormalities in Alzheimer disease

Robert B. Petersen, George Perry, Shun Shimohama, 2000, Neurobiology of Aging.

PEROXISOMAL ABNORMALITIES IN METABOLIC DISEASES

Anne B. Johnson, E. Essner, S. Goldfischer, 1973, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Ganglioside localization in cerebellar cortex: an immunoperoxidase study with antibody to GM1 ganglioside

M. Naiki, Anne B. Johnson, D. Marcus, 1976, Brain Research.

EVIDENCE THAT ALZHEIMER NEUROFIBRILLARY TANGLES ORIGINATE FROM NEUROTUBULES

R. Terry, I. Grundke‐Iqbal, K. Iqbal, 1979, The Lancet.

STUDIES ON BRAIN BIOPSIES OF PATIENTS WITH HUNTINGTON'S CHOREA

R. Terry, Anne B. Johnson, 1974, Journal of neuropathology and experimental neurology.

Striated adrenocortical cells in cerebro-hepato-renal (Zellweger) syndrome

H. Moser, J. Powers, F. R. Brown, 2004, Virchows Archiv A.

Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome

I. Rapin, A. Spiro, M. Valsamis, 1973, Science.

Granulofilamentous inclusions in a meningioma

J. Goldman, D. Horoupian, Anne B. Johnson, 1980, Cancer.

Alexander Disease: New Insights From Genetics

J. Goldman, A. Messing, M. Brenner, 2001, Journal of neuropathology and experimental neurology.

Alexander Disease: A Leukodystrophy Caused by a Mutation in GFAP

Anne B. Johnson, 2004, Neurochemical Research.

Alexander's Disease

M. Brenner, Anne B. Johnson, 2003, Journal of child neurology.

Alexander disease: a review and the gene

Anne B. Johnson, 2002, International Journal of Developmental Neuroscience.

Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome

R. Schiffmann, R. Matalon, R. Armstrong, 2000, Acta Neuropathologica.

Vesicular disruption of myelin in autoimmune demyelination

H. Wiśniewski, C. Raine, S. Brostoff, 1975, Journal of the Neurological Sciences.

Demyelination in vitro Absorption studies demonstrate that galactocerebroside is a major target

C. Raine, A. Suzuki, M. Bornstein, 1981, Journal of the Neurological Sciences.

Experimental allergic encephalomyelitis Characterization of serum factors causing demyelination and swelling of myelin

C. Brosnan, I. Grundke‐Iqbal, C. Raine, 1981, Journal of the Neurological Sciences.

GM2-Gangliosidosis, AB variant

I. Rapin, Kinuko Suzuki, Anne B. Johnson, 1975, Acta Neuropathologica.

A marker for oligodendrocytes and its relation to myelinogenesis: An immunocytochemical study with experimental allergic encephalomyelitis serum and C.N.S. cultures

C. Raine, M. Bornstein, Anne B. Johnson, 1981, Journal of neurocytology.

Effects of anti-white matter serum on myelin and lipid synthesis in brain prisms

C. Raine, M. Bornstein, Anne B. Johnson, 1979, Brain Research.

Myelin-binding antibodies in vitro. Immunoperoxidase studies with experimental allergic encephalomyelitis, anti-galactocerebroside and multiple sclerosis sera

M. Bornstein, Anne B. Johnson, 1978, Brain Research.

Third International Congress of Histochemistry and Cytochemistry: August 18–22, 1968, New York, N.Y.

W. D. Selles, W. W. Doane, J. E. Kephart, 1968 .

Third International Congress of Histochemistry and Cytochemistry

Richard E. Cornell, W. D. Selles, W. W. Doane, 1968 .

Purification, Characterization, and Localization of Aspartoacylase from Bovine Brain

R. Kaul, Peter Q. Tang, R. Matalon, 1991, Journal of neurochemistry.

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

D. Rodriguez, O. Boespflug-Tanguy, J. Goldman, 2001, Nature Genetics.

Propensity for paternal inheritance of de novo mutations in Alexander disease

M. Knaap, D. Rodriguez, O. Boespflug-Tanguy, 2006, Human Genetics.

Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease

B. Banwell, S. Naidu, R. Weller, 2005, Annals of neurology.

Microtubule reduction in Alzheimer's disease and aging is independent of tau filament formation.

George Perry, Xiongwei Zhu, Gjumrakch Aliev, 2003, The American journal of pathology.

Deficiency of ATPase-Positive Astrocytic Processes in Spongy Degeneration of the Nervous System (Canavanʼs Disease)

Anne B. Johnson, 1970 .

Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease.

J. Moffett, P. Arun, C. N. Madhavarao, 2005, Proceedings of the National Academy of Sciences of the United States of America.

AMPA receptor protein expression and function in astrocytes cultured from hippocampus

R. Araneda, R. Zukin, J. Kessler, 1999, Journal of neuroscience research.

MITOCHONDRIA ABNORMALITIES MARK VULNERABLE NEURONS IN ALZHEIMER DISEASE

H. Vinters, A. Nunomura, Mark A. Smith, 1999 .

Alzheimer neurofibrillary tangles: Antiserum and immunohistological staining

Khadija Iqbal, H. Wiśniewski, R. Terry, 1979, Annals of neurology.

Genomic alterations in cervical carcinoma: losses of chromosome heterozygosity and human papilloma virus tumor status.

H. Klinger, R. Burk, M. Mullokandov, 1996, Cancer research.

Alexander disease: new insights from genetics.

J. Goldman, A. Messing, M. Brenner, 2001 .

ASPARTOACYLASE, THE DEFICIENT ENZYME IN SPONGY DEGENERATION (CANAVAN DISEASE), IS A MYELIN-ASSOCIATED ENZYME: 144

R. Kaul, R. Matalon, Anne B. Johnson, 1989 .

A case of juvenile lipidosis: Electron microscopic, histochemical and biochemical studies

K. Suzuki, Kinuko Suzuki, Anne B. Johnson, 1968, Acta Neuropathologica.

Multiple sclerosis, Guillain–Barré syndrome and myelin basic protein-specific cellular antibody

Anne B. Johnson, M. Canto, 1976, Nature.