Anvret, M: search on Z-Library

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1

Huntington Disease Phenocopy Is a Familial Prion Disease

Richard C. Moore, Fengqing Xiang, Jeffrey Monaghan, Dong Han, Zhiping Zhang, Lars Edström, Maria Anvret, Stanley B. Prusiner

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 54 KB

english, 2001

2

Reply to Dr. Benedetti et al

Dr. Maria Anvret, Jan Wahlström

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 52 KB

english, 1992

3

Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family

Maria Anvret, Christopher Gillberg, Jan Wahlström, Kerstin Albertsson-Wikland, Kay Davies

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 396 KB

english, 1988

4

Characterization of the von Willebrand Factor Gene (VWF) in von Willebrand Disease Type III Patients from 24 Families of Swedish and Finnish Origin

Z.P. Zhang, M. Blombäck, N. Egberg, G. Falk, M. Anvret

Journal:

Year:

1994

File:

PDF, 472 KB

1994

5

Reactions to predictive testing in Huntington disease: Case reports of coping with a new genetic status

Wahlin, Tarja-Brita Robins, Lundin, Anders, Bäckman, Lars, Almqvist, Elisabeth, Haegermark, Aina, Winblad, Bengt, Anvret, Maria

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 158 KB

english, 1997

6

A novel missense mutation Ile538Val in the fibroblast growth factor receptor 3 in hypochondroplasia

G Grigelioniené, L Hagenäs, O Eklöf, L Neumeyer, PE Haereid, M Anvret

Journal:

Year:

1998

Language:

english

File:

PDF, 117 KB

english, 1998

7

Genetic linkage of Welander distal myopathy to chromosome 2p13

Gabrielle Åhlberg, Désirée Von Tell, Kristian Borg, Lars Edström, Maria Anvret

Journal:

Annals of Neurology

Year:

1999

Language:

english

File:

PDF, 487 KB

english, 1999

8

Alcohol dehydrogenase alleles in Parkinson's disease

Silvia Buervenich, Olof Sydow, Andrea Carmine, Zhiping Zhang, Maria Anvret, Lars Olson

Journal:

Movement Disorders

Year:

2000

Language:

english

File:

PDF, 43 KB

english, 2000

9

On laboratory problems in diagnosing mild von Willebrand's disease

M. Blombäck, P. Eneroth, O. Andersson, M. Anvret

Journal:

American Journal of Hematology

Year:

1992

Language:

english

File:

PDF, 307 KB

english, 1992

10

Chromosome findings in the rett syndrome and a test of a two-step mutation theory

Jan Wahlström, Maria Anvret, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 383 KB

english, 1986

11

Segregation analysis of the X-chromosome in a family with rett syndrome in two generations

Maria Anvret, Dr. Jan Wahlström, Per Skogsberg, Bengt Hagberg

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 457 KB

english, 1990

12

Aicardi syndrome: Early neuroradiological manifestations and results of DNA studies in one patient

Karen Bröndum Nielsen, Maria Anvret, Olof Flodmark, Peter Furuskog, Kjersti Bohman-Valis

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 401 KB

english, 1991

13

Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13

Karen Heleneörstavik, Svein Erik Tangsrud, Ragnhild Kiil, Inger-Lise Hansteen, Jon Steen-Johnsen, Suzanne B. Cassidy, Anna Martony, Maria Anvret, Niels Tommerup, Karen Bröndum-Nielsen

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 487 KB

english, 1992

14

NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits

Andrea Carmine, Silvia Buervenich, Dagmar Galter, Erik G. Jönsson, Göran C. Sedvall, Lars Farde, J. Petter Gustavsson, Hans Bergman, Kodavali V. Chowdari, Vishwajit L. Nimgaonkar, Maria Anvret, Olof S

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2003

Language:

english

File:

PDF, 84 KB

english, 2003

15

Identification of four novel polymorphisms in the calcitonin/α-CGRP (CALCA) gene and an investigation of their possible associations with Parkinson disease, schizophrenia, and manic depression

Silvia Buervenich, Fengqing Xiang, Olof Sydow, Erik G. Jönsson, Göran C. Sedvall, Maria Anvret, Lars Olson

Journal:

Year:

2001

Language:

english

File:

PDF, 197 KB

english, 2001

16

Relationship between the Epstein-Barr virus and undifferentiated nasopharyngeal carcinoma: Correlated nucleic acid hybridization and histopathological examination

Maria Andersson-Anvret, Nils Forsby, George Klein, Werner Henle

Journal:

International Journal of Cancer

Year:

1977

Language:

english

File:

PDF, 736 KB

english, 1977

17

Chromosome banding, isoenzyme studies and determination of epstein-barr virus DNA content on human burkitt lymphoma/mouse hybrids

Jack Spira, Susanne Povey, Francis Wiener, George Klein, Maria Andersson-Anvret

Journal:

International Journal of Cancer

Year:

1977

Language:

english

File:

PDF, 423 KB

english, 1977

18

14q+ marker chromosome in an EBV-genome-negative lymph node without signs of malignancy in a patient with EBV-genome-positive nasopharyngeal carcinoma

F. Mitelman, G. Klein, M. Andersson-Anvret, N. Forsby, B. Johansson

Journal:

International Journal of Cancer

Year:

1979

Language:

english

File:

PDF, 473 KB

english, 1979

19

Relationship between the Epstein-Barr virus genome and nasopharyngeal carcinoma in Caucasian patients

Maria Andersson-Anvret, Nils Forsby, George Klein, Werner Henle, Anders Biörklund

Journal:

International Journal of Cancer

Year:

1979

Language:

english

File:

PDF, 511 KB

english, 1979

20

Reciprocal 8;14 translocation in EBV-negative B-cell acute lymphocytic leukemia with burkitt-type cells

F. Mitelman, M. Andersson-Anvret, L. Brandt, D. Catovsky, G. Klein, G. Manolov, Y. Manolova, E. Mark-Vendel, P. G. Nilsson

Journal:

International Journal of Cancer

Year:

1979

Language:

english

File:

PDF, 1.12 MB

english, 1979

21

Relationship between the amounts of EBV-DNA and ebna per cell, clonability and tumorigenicity in two EBV-negative lymphoma lines and their EBV-converted sublines

I. Ernberg, G. Klein, B. C. Giovanella, J. Stehlin, K. J. McCormick, M. Andersson-Anvret, P. Åman, D. Killander

Journal:

International Journal of Cancer

Year:

1983

Language:

english

File:

PDF, 631 KB

english, 1983

22

Constitutional and somatic mutations in the WTI gene in wilms' tumor patients

Agneta Nordenskjöld, Eitan Friedman, Bengt Sandstedt, Stefan Söderhäll, Maria Anvret

Journal:

International Journal of Cancer

Year:

1995

Language:

english

File:

PDF, 1.61 MB

english, 1995

23

Epstein-barr virus in somatic cell hybrids between mouse cells and human nasopharyngeal carcinoma cells

Zenon Steplewski, Hilary Koprowski, Maria Andersson-Anvret, George Klein

Journal:

Journal of Cellular Physiology

Year:

1978

Language:

english

File:

PDF, 618 KB

english, 1978

24

Further evidence for an association of the Paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease

Andrea Carmine, Silvia Buervenich, Olof Sydow, Maria Anvret, Lars Olson

Journal:

Movement Disorders

Year:

2002

Language:

english

File:

PDF, 54 KB

english, 2002

25

MECP2 mutations in Swedish Rett syndrome clusters

F Xiang, Y Stenbom, M Anvret

Journal:

Clinical Genetics

Year:

2002

Language:

english

File:

PDF, 25 KB

english, 2002

26

High suicidal ideation in persons testing for Huntington's disease

T-B. Robins Wahlin, L. Bäckman, A. Lundin, A. Haegermark, B. Winblad, M. Anvret

Journal:

Acta Neurologica Scandinavica

Year:

2000

Language:

english

File:

PDF, 196 KB

english, 2000

27

CTG-repeat length in distal and proximal leg muscles of symptomatic and non-symptomatic patients with myotonic dystrophy: relation to muscle strength and degree of histopathological abnormalities

Birgitta Hedberg, Maria Anvret, Tor Ansved

Journal:

European Journal of Neurology

Year:

1999

File:

PDF, 1.26 MB

1999

28

Effects of the mutant von Willebrand factor gene in von Willebrand disease

Zhiping Zhang, Monica Lindstedt, Margareta Blombäck, Maria Anvret

Journal:

Year:

1995

Language:

english

File:

PDF, 663 KB

english, 1995

29

Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the “critical segment” towards the telomere

Maria Anvret, Magnus Nordenskjöld, Lisa Stolpe, Lena Johansson, Karen Bröndum-Nielsen

Journal:

Year:

1991

Language:

english

File:

PDF, 241 KB

english, 1991

30

Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyria

Jin-Sung Lee, Gunnel Lundin, Maria Anvret, Lars Lannfelt, Lotta Forsell, Christiane Picat, Bernard Grandchamp

Journal:

Year:

1991

Language:

english

File:

PDF, 587 KB

english, 1991

31

Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reaction

Jin-Sung Lee, Jan Lindsten, Maria Anvret

Journal:

Year:

1990

Language:

english

File:

PDF, 393 KB

english, 1990

32

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations

N. Archidiacono, M. Lerone, M. Rocchi, M. Anvret, T. Ozcelik, U. Francke, G. Romeo

Journal:

Year:

1991

Language:

english

File:

PDF, 452 KB

english, 1991

33

Geographical distribution of haplotypes in Swedish families with Huntington's disease

Elisabeth Almqvist, Susan Andrew, Jane Theilmann, Paul Goldberg, Jutta Zeisler, Ulf Drugge, Ulla Grandell, Margareta Tapper-Persson, Bengt Winblad, Michael Hayden, Maria Anvret

Journal:

Year:

1994

Language:

english

File:

PDF, 526 KB

english, 1994

34

A normal male with an inherited deletion of one exon within the DMD gene

Magnus Nordenskjöld, Louise Nicholson, Lars Edström, Maria Anvret, Maria Eiserman, Clarke Slater, Lisa Stolpe

Journal:

Year:

1990

Language:

english

File:

PDF, 551 KB

english, 1990

35

WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin

Agneta Nordenskjöld, Eitan Friedman, Maria Anvret

Journal:

Year:

1994

Language:

english

File:

PDF, 803 KB

english, 1994

36

394delTT: a Nordic cystic fibrosis mutation

Marianne Schwartz, Maria Anvret, Mireille Claustres, Hans Geir Eiken, Kristin Eiklid, Charlotte Schaedel, Lisa Stolpe, Lisbeth Tranebjærg

Journal:

Year:

1994

Language:

english

File:

PDF, 624 KB

english, 1994

37

Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesis

A. Nordenskjöld, G. Fricke, M. Anvret

Journal:

Year:

1995

Language:

english

File:

PDF, 334 KB

english, 1995

38

Genetic and blood coagulation characterization of “Swedish” families with von Willebrand's disease types I and III: New aspects of heredity

Maria Anvret, Margareta Blombäck, Monika Lindstedt, Elisabeth Söderlind, Margareta Tapper-Persson, Ann-Christine Thelander

Journal:

Year:

1992

Language:

english

File:

PDF, 728 KB

english, 1992

39

X chromosome linkage studies in familial Rett syndrome

Andrew R. J. Curtis, Sophie Headland, Susan Lindsay, Nicholas S. T. Thomas, Eileen Boye, Smaragda Kamakari, Paul Roustan, Maria Anvret, Jan Wahlstrom, Gillian McCarthy, Angus J. Clarke, Shomi Bhattach

Journal:

Year:

1993

Language:

english

File:

PDF, 428 KB

english, 1993

40

Two new mutations in the porphobilinogen deaminase gene and a screening method using PCR amplification of specific alleles

Gunnel Lundin, Anna Wedell, Stig Thunell, Maria Anvret

Journal:

Year:

1994

Language:

english

File:

PDF, 545 KB

english, 1994

41

Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene

L. Osborne, G. Santis, M. Schwarz, K. Klinger, T. Dörk, I. McIntosh, M. Schwartz, V. Nunes, M. Macek, J. Reiss, W. E. Highsmith, R. McMahon, G. Novelli, N. Malik, J. Bürger, M. Anvret, A. Wallace, C.

Journal:

Year:

1992

Language:

english

File:

PDF, 590 KB

english, 1992

42

Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q

K. Johnson, E. Nimmo, P. Jones, M. Weiss, M. -L. Savontaus, M. Anvret, R. Bartlett, A. Roses, D. Shaw, P. S. Harper, E. Koivunen-Tapio, R. Williamson

Journal:

Year:

1988

Language:

english

File:

PDF, 360 KB

english, 1988

43

DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyria

Jin-Sung Lee, Maria Anvret, Jan Lindsten, Lars Lannfelt, Pär Gellerfors, Lennart Wetterberg, Ylva Floderus, Stig Thunell

Journal:

Year:

1988

Language:

english

File:

PDF, 286 KB

english, 1988

44

DNA linkage analysis of X-linked retinoschisis

N. Dahl, P. Goonewardena, J. Chotai, M. Anvret, U. Pettersson

Journal:

Year:

1988

Language:

english

File:

PDF, 343 KB

english, 1988

45

Dopamine D1receptor number — a sensitive PET marker for early brain degeneration in Huntington's disease

Göran Sedvall, Per Karlsson, Anders Lundin, Maria Anvret, Tetsuya Suhara, Christer Halldin, Lars Farde

Journal:

European Archives of Psychiatry and Clinical Neuroscience

Year:

1994

Language:

english

File:

PDF, 2.65 MB

english, 1994

46

Complex genetic counseling and exclusion of duchenne muscular dystrophy in a twin pregnancy after in vitro fertilization (IVF)

The-Hung Bui, Maria Anvret, Niklas Dahl, Leena Garoff, Peter Sjöblom, Torbjörn Hillensjö

Journal:

Journal of Assisted Reproduction and Genetics

Year:

1994

Language:

english

File:

PDF, 437 KB

english, 1994

47

Screening for mutations in candidate genes for hypospadias

Agenta Nordenskjöld, Eitan Friedman, Margareta Tappar-Persson, Cilla Söderhäll, Amos Leviav, Jan Svensson, Maria Anvret

Journal:

Year:

1999

Language:

english

File:

PDF, 636 KB

english, 1999

48

Genetic investigation of the porphobilinogen deaminase gene in Swedish acute intermittent porphyria families

Gunnel Lundin, Jin-Sung Lee, Stig Thunell, M. Anvret

Journal:

Year:

1997

Language:

english

File:

PDF, 33 KB

english, 1997

49

Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B)

P.-J. Svensson, Maria Anvret, Marie-Louise Molander, Agneta Nordenskjöld

Journal:

Year:

1998

Language:

english

File:

PDF, 66 KB

english, 1998

50

Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of theDYSFlocus

Désirée Tell, CarlE.G. Bruder, LouiseV.B. Anderson, Maria Anvret, Gabrielle Åhlberg

Journal:

Year:

2003

Language:

english

File:

PDF, 293 KB

english, 2003

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