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Barbara Levinson

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Allison Gregory; Shawn K Westaway; I E Holm; P T Kotzbauer; Penelope Hogarth; S Sonek; J C Coryell; T M Nguyen; Nardo Nardocci; G Zorzi; Dayana D Rodriguez; I Desguerre; Enrico Bertini; A Simonati; Barbara Levinson; C Dias; C Barbot; I Carrilho; M Santos; I Malik; Jane Gitschier; Susan J Hayflick
Neurodegeneration associated with genetic defects in phospholipase A(2).
E Alexandra Athos; Barbara Levinson; Amy L Kistler; Jason Zemansky; Alan Bostrom; Nelson B Freimer; Jane Gitschier
Dichotomy and perceptual distortions in absolute pitch ability.
Shawn K Westaway; Katherine H L Ching; Barbara Levinson; Jane Gitschier; Susan J Hayflick
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).

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All Publications

2008: Allison Gregory; Shawn K Westaway; I E Holm; P T Kotzbauer; Penelope Hogarth; S Sonek; J C Coryell; T M Nguyen; Nardo Nardocci; G Zorzi; Dayana D Rodriguez; I Desguerre; Enrico Bertini; A Simonati; Barbara Levinson; C Dias; C Barbot; I Carrilho; M Santos; I Malik; Jane Gitschier; Susan J Hayflick
Neurodegeneration associated with genetic defects in phospholipase A(2).
Neurology 2008;71(18):1402-9.
2007: E Alexandra Athos; Barbara Levinson; Amy L Kistler; Jason Zemansky; Alan Bostrom; Nelson B Freimer; Jane Gitschier
Dichotomy and perceptual distortions in absolute pitch ability.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(37):14795-800.
2006: Shawn K Westaway; Katherine H L Ching; Barbara Levinson; Jane Gitschier; Susan J Hayflick
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
Human genetics 2006;119(6):679.
2006: Shawn K Westaway; Katherine H L Ching; Barbara Levinson; Jane Gitschier; Susan J Hayflick
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
Human genetics 2006;119(6):678.
2006: Shawn K Westaway; Katherine H L Ching; Barbara Levinson; J G Gitschier; Susan J Hayflick
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
Human genetics 2006;119(6):677.
2006: Shawn K Westaway; Katherine H L Ching; Barbara Levinson; Jane Gitschier; Susan J Hayflick
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
Human genetics 2006;119(6):673.
2006: Shawn K Westaway; Katherine H L Ching; Barbara Levinson; Jane Gitschier; Susan J Hayflick
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
Human genetics 2006;119(6):672.
2006: Shawn K Westaway; Katherine H L Ching; Barbara Levinson; Jane Gitschier; Susan J Hayflick
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
Human genetics 2006;119(6):671-2.
2006: Neil V Morgan; Shawn K Westaway; Jenny E V Morton; Allison Gregory; Paul Gissen; Scott Sonek; Hakan Cangul; Jason Coryell; Natalie Canham; Nardo Nardocci; Giovanna Zorzi; Shanaz Pasha; Diana Rodriguez; Isabelle Desguerre; Ammar F Mubaidin; Enrico Bertini; Richard C Trembath; Alessandro Simonati; Carolyn Schanen; Colin A Johnson; Barbara Levinson; C Geoffrey Woods; Beth Wilmot; Patricia L Kramer; Jane Gitschier; Eamonn R Maher; Susan J Hayflick
PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron.
Nature genetics 2006;38(7):752-4.
2003: Susan J Hayflick; Shawn K Westaway; Barbara Levinson; Bing Zhou; Monique A Johnson; Katherine H L Ching; Jane Gitschier
Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
The New England journal of medicine 2003;348(1):33-40.
2001: B Zhou; S K Bae; A C Malone; Barbara Levinson; Y M Kuo; M R Cilio; E Bertini; Susan J Hayflick; Jane Gitschier
hGFRalpha-4: a new member of the GDNF receptor family and a candidate for NBIA.
Pediatric neurology 2001;25(2):156-61.
2001: B Zhou; Shawn K Westaway; Barbara Levinson; Monique A Johnson; Jane Gitschier; Susan J Hayflick
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome.
Nature genetics 2001;28(4):345-9.
1997: Y Murata; Hiroko Kodama; Takanori Abe; N Ishida; M Nishimura; Barbara Levinson; Jane Gitschier; Seymour Packman
Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease.
Pediatric research 1997;42(4):436-42.
1997: Barbara Levinson; Seymour Packman; Jane Gitschier
Deletion of the promoter region in the Atp7a gene of the mottled dappled mouse.
Nature genetics 1997;16(3):224-5.
1996: Barbara Levinson; R Conant; R Schnur; S Das; Seymour Packman; Jane Gitschier
A repeated element in the regulatory region of the MNK gene and its deletion in a patient with occipital horn syndrome.
Human molecular genetics 1996;5(11):1737-42.
1996: Stephen G Kaler; S Das; Barbara Levinson; David S Goldstein; C S Holmes; N J Patronas; Seymour Packman; William A Gahl
Successful early copper therapy in Menkes disease associated with a mutant transcript containing a small In-frame deletion.
Biochemical and molecular medicine 1996;57(1):37-46.
1995: B S Chortkoff; C T Gonsowski; H L Bennett; Barbara Levinson; D P Crankshaw; Robert C Dutton; P Ionescu; R I Block; Edmond I Eger
Subanesthetic concentrations of desflurane and propofol suppress recall of emotionally charged information.
Anesthesia and analgesia 1995;81(4):728-36.
1995: S Das; Barbara Levinson; C Vulpe; S Whitney; Jane Gitschier; Seymour Packman
Similar splicing mutations of the Menkes/mottled copper-transporting ATPase gene in occipital horn syndrome and the blotchy mouse.
American journal of human genetics 1995;56(3):570-6.
1995: S Das; S Whitney; J Taylor; E Chen; Barbara Levinson; C Vulpe; Jane Gitschier; Seymour Packman
Prenatal diagnosis of Menkes disease by mutation analysis.
Journal of inherited metabolic disease 1995;18(3):364-5.
1994: S Das; Barbara Levinson; S Whitney; C Vulpe; Seymour Packman; Jane Gitschier
Diverse mutations in patients with Menkes disease often lead to exon skipping.
American journal of human genetics 1994;55(5):883-9.
1994: Barbara Levinson; C Vulpe; B Elder; C Martin; F Verley; Seymour Packman; Jane Gitschier
The mottled gene is the mouse homologue of the Menkes disease gene.
Nature genetics 1994;6(4):369-73.
1993: C Vulpe; Barbara Levinson; S Whitney; Seymour Packman; Jane Gitschier
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase.
Nature genetics 1993;3(1):7-13.
1993: Barbara Levinson; Jane Gitschier; C Vulpe; S Whitney; S Yang; Seymour Packman
Are X-linked cutis laxa and Menkes disease allelic?
Nature genetics 1993;3(1):6.
1992: Barbara Levinson; Sue Kenwrick; P Gamel; K Fisher; Jane Gitschier
Evidence for a third transcript from the human factor VIII gene.
Genomics 1992;14(3):585-9.
1992: C J Faust; Barbara Levinson; Jane Gitschier; Gail E Herman
Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage.
Genomics 1992;13(4):1289-95.
1992: Barbara Levinson; John bermingham; A Metzenberg; Sue Kenwrick; Verne M Chapman; Jane Gitschier
Sequence of the human factor VIII-associated gene is conserved in mouse.
Genomics 1992;13(3):862-5.
1992: Sue Kenwrick; Barbara Levinson; S Taylor; Amy D Shapiro; Jane Gitschier
Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII gene.
Human molecular genetics 1992;1(3):179-86.
1992: S Jonsdottir; C Diamond; Barbara Levinson; S Magnusson; O Jensson; Jane Gitschier
Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresis.
Human mutation 1992;1(6):506-8.
1992: C Diamond; Scott C Kogan; Barbara Levinson; Jane Gitschier
Amino acid substitutions in conserved domains of factor VIII and related proteins: study of patients with mild and moderately severe hemophilia A.
Human mutation 1992;1(3):248-57.
1991: Jane Gitschier; Scott C Kogan; C Diamond; Barbara Levinson
Genetic basis of hemophilia A.
Thrombosis and haemostasis 1991;66(1):37-9.
1990: Barbara Levinson; Sue Kenwrick; D Lakich; G Hammonds; Jane Gitschier
A transcribed gene in an intron of the human factor VIII gene.
Genomics 1990;7(1):1-11.
1990: Barbara Levinson; A E Lehesjoki; A de la Chapelle; Jane Gitschier
Molecular analysis of hemophilia A mutations in the Finnish population.
American journal of human genetics 1990;46(1):53-62.
1989: Jane Gitschier; Barbara Levinson; A E Lehesjoki; A De La Chapelle
Mosaicism and sporadic haemophilia: implications for carrier determination.
Lancet 1989;1(8632):273-4.
1988: Jane Gitschier; Scott C Kogan; Barbara Levinson; E G Tuddenham
Mutations of factor VIII cleavage sites in hemophilia A.
Blood 1988;72(3):1022-8.
1987: Barbara Levinson; R Janco; J Phillips; Jane Gitschier
A novel missense mutation in the factor VIII gene identified by analysis of amplified hemophilia DNA sequences.
Nucleic acids research 1987;15(23):9797-805.