Search Results - "Johnson, Anne B"

Mitochondrial Abnormalities in Alzheimer's Disease by Hirai, Keisuke, Aliev, Gjumrakch, Nunomura, Akihiko, Fujioka, Hisashi, Russell, Robert L, Atwood, Craig S, Johnson, Anne B, Kress, Yvonne, Vinters, Harry V, Tabaton, Massimo, Shimohama, Shun, Cash, Adam D, Siedlak, Sandra L, Harris, Peggy L. R, Jones, Paul K, Petersen, Robert B, Perry, George, Smith, Mark A

“…The finding that oxidative damage, including that to nucleic acids, in Alzheimer's disease is primarily limited to the cytoplasm of susceptible neuronal…”
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Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease by Li, Rong, Johnson, Anne B., Salomons, Gajja, Goldman, James E., Naidu, Sakkubai, Quinlan, Roy, Cree, Bruce, Ruyle, Stephanie Z., Banwell, Brenda, D'Hooghe, Marc, Siebert, Joseph R., Rolf, Cristin M., Cox, Helen, Reddy, Alyssa, Gutiérrez-Solana, Luis González, Collins, Amanda, Weller, Roy O., Messing, Albee, van der Knaap, Marjo S., Brenner, Michael

“…Alexander disease is a progressive, usually fatal neurological disorder defined by the widespread and abundant presence in astrocytes of protein aggregates…”
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Carotid-femoral pulse wave velocity is negatively correlated with aortic diameter by Bailey, Marc A, Davies, Jennifer M, Griffin, Kathryn J, Bridge, Katherine I, Johnson, Anne B, Sohrabi, Soroush, Baxter, Paul D, Scott, D Julian A

“…Cardiovascular events pose significant morbidity and mortality burden to abdominal aortic aneurysm (AAA) patients. Arterial stiffness as measured by pulse wave…”
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Plasma thrombin-antithrombin complex, prothrombin fragments 1 and 2, and D-dimer levels are elevated after endovascular but not open repair of infrarenal abdominal aortic aneurysm by Bailey, Marc A., MB, ChB, BSc, MRCS, Griffin, Kathryn J., MB, Bchir, MA, MRCS, Sohrabi, Soroush, PhD, MRCS, Whalley, Daniel J., BSc, MRes, Johnson, Anne B., RN, Baxter, Paul D., PhD, CStat, Ariëns, Robert A.S., BSc, PhD, Scott, D. Julian A., MD, FRCS, FRCS(Ed), FEBVS

“…Introduction Abdominal aortic aneurysm (AAA) is associated with hypercoagulability, evidenced by increased markers of coagulation activation, including…”
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Propensity for paternal inheritance of de novo mutations in Alexander disease by RONG LI, JOHNSON, Anne B, SALOMONS, Gajja S, VAN DER KNAAP, Marjo S, RODRIGUEZ, Diana, BOESPFLUG-TANGUY, Odile, GOROSPE, J. Rafael, GOLDMAN, James E, MESSING, Albee, BRENNER, Michael

“…De novo dominant mutations in the GFAP gene have recently been associated with nearly all cases of Alexander disease, a rare but devastating neurological…”
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Alexander disease: a leukodystrophy caused by a mutation in GFAP by Johnson, Anne B

“…Alexander disease, a rare fatal disorder of the central nervous system, causes progressive loss of motor and mental function. Until recently it was of unknown…”
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Alexander disease: a review and the gene by Johnson, Anne B.

“…This review presents historical and clinical information on the rare human brain disorder known as Alexander disease (ALX), and reports on the recent discovery…”
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Mutations in GFAP , encoding glial fibrillary acidic protein, are associated with Alexander disease by Messing, Albee, Brenner, Michael, Boespflug-Tanguy, Odile, Johnson, Anne B, Goldman, James E, Rodriguez, Diana

“…Alexander disease is a rare disorder of the central nervous system of unknown etiology. Infants with Alexander disease develop a leukoencephalopathy with…”
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Microtubule Reduction in Alzheimer's Disease and Aging Is Independent of τ Filament Formation by Cash, Adam D., Aliev, Gjumrakch, Siedlak, Sandra L., Nunomura, Akihiko, Fujioka, Hisashi, Zhu, Xiongwei, Raina, Arun K., Vinters, Harry V., Tabaton, Massimo, Johnson, Anne B., Paula-Barbosa, Manuel, Avíla, Jesus, Jones, Paul K., Castellani, Rudy J., Smith, Mark A., Perry, George

“…Biochemical studies show that phosphorylated τ, like that found in paired helical filaments (PHFs), does not promote microtubule assembly leading to the view…”
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Calcium channel blockers enhance sac shrinkage after endovascular aneurysm repair by Bailey, Marc A., MRCS, Sohrabi, Soroush, PhD, Flood, Karen, FRCR, Griffin, Kathryn J., MRCS, Rashid, S. Tawqeer, PhD, Johnson, Anne B, Baxter, Paul D., PhD, Patel, Jai V., FRCR, Scott, D. Julian A., MD

“…Objective Sac shrinkage is a surrogate marker of success after endovascular aneurysm repair (EVAR). We set out to determine if any common cardioprotective…”
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Alexander's Disease: Clinical, Pathologic, and Genetic Features by Johnson, Anne B., Brenner, Michael

“…Alexander's disease, a rare and fatal disorder of the central nervous system, most commonly affects infants and young children but can also occur in older…”
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Alexander Disease: New Insights From Genetics by MESSING, ALBEE, GOLDMAN, JAMES E, JOHNSON, ANNE B, BRENNER, MICHAEL

“…Prior to finding that GFAP mutations underlie many cases of Alexander disease, it was unclear whether the disease originated in astrocytes or if the formation…”
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Modeling the Growth of Infrarenal Abdominal Aortic Aneurysms by Bailey, Marc A, Baxter, Paul D, Jiang, Tao, Charnell, Aimee M, Griffin, Kathryn J, Johnson, Anne B, Bridge, Katherine I, Sohrabi, Soroush, Scott, D Julian A

“…Abdominal aortic aneurysm (AAA) growth is a complex process that is incompletely understood. Significant heterogeneity in growth trajectories between patients…”
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Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome by KONDI WONG, ARMSTRONG, Regina C, BRADLEY, Courtney A, CRUTCHFIELD, Kevin, SCHIFFMANN, Raphael, GYURE, Kymberly A, MORRISON, Alan L, RODRIGUEZ, Diana, MATALON, Reuben, JOHNSON, Anne B, WOLLMANN, Robert, GILBERT, Enid, LE, Tuan Q

“…Childhood ataxia with diffuse central nervous system hypomyelination syndrome (CACH) is a recently described leukodystrophy of unknown etiology. To…”
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Genomic alterations in cervical carcinoma : losses of chromosome heterozygosity and human papilloma virus tumor status by MULLOKANDOV, M. R, KHOLODILOV, N. G, ATKIN, N. B, BURK, R. D, JOHNSON, A. B, KLINGER, H. P

“…Specific human papilloma virus (HPV) types appear to be necessary etiological factors for most cervical cancers, yet additional genetic alterations seem to be…”
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Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome by Goldfischer, Sidney, Moore, Cyril L., Johnson, Anne B., Spiro, Alfred J., Valsamis, Marius P., Wisniewski, Henry K., Ritch, Robert H., Norton, William T., Rapin, Isabelle, Gartner, Lawrence M.

“…The cerebro-hepato-renal syndrome is a rare familial malady with cerebral, renal, and skeletal abnormalities, severe hypotonia, cirrhosis, iron and lipid…”
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Purification, characterization, and localization of aspartoacylase from bovine brain by Kaul, R, Casanova, J, Johnson, A B, Tang, P, Matalon, R

“…Canavan disease, an autosomal recessive disorder, is characterized biochemically by N-acetylaspartic aciduria and aspartoacylase (N-acyl-L-aspartate…”
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Genetic spongiform encephalopathies by Johnson, A B

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Studies on brain biopsies of patients with Huntington's chorea by Tellez-Nagel, I, Johnson, A B, Terry, R D

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Multiple sclerosis, Guillain-Barré syndrome and myelin basic protein-specific cellular antibody by JOHNSON, ANNE B, CANTO, MAURO C. DAL

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