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1

Fragile X families in a Northern Swedish county - a genealogical study demonstrating apparent paternal transmission from the 18th century

Gösta Holmgren, Hans K. Son Blomquist, Ulf Drugge, Karl-Henrik Gustavson

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 276 KB

english, 1988

2

Study of individuals possibly affected with the fragile X syndrome in a large swedish family in the 18th to 20th centuries

Ulf Drugge, GöSta Holmgren, Hans Kison Blomquist, Niklas Dahl, Karl-Henrik Gustavson, Helena Malmgren

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 157 KB

english, 1992

3

Clinical and electroencephalographic characteristics of epilepsy in rural Ethiopia: a community-based study

Redda Tekle-Haimanot, Lars Forsgren, Mekonnen Abebe, Ayele Gebre-Mariam, Jan Heijbel, Gösta Holmgren, Jan Ekstedt

Journal:

Epilepsy Research

Year:

1990

Language:

english

File:

PDF, 1.14 MB

english, 1990

4

Attitudes of rural people in central Ethiopia toward epilepsy

Redda Tekle-Haimanot, Mekonnen Abebe, Lars Forsgren, Ayele Gebre-Mariam, Jan Heijbel, Gösta Holmgren, Jan Ekstedt

Journal:

Social Science & Medicine

Year:

1991

Language:

english

File:

PDF, 743 KB

english, 1991

5

Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study

Ola Sandgren, Ulf Drugge, Gösta Holmgren, Alda Sousa

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 518 KB

english, 1991

6

Coexpression of the sis and myc proto-oncogenes in developing human placenta suggests autocrine control of trophoblast growth

Goustin, Anton Scott, Betsholtz, Christer, Pfeifer-Ohlsson, Susan, Persson, Håkan, Rydnert, Jan, Bywater, Margaret, Holmgren, Gösta, Heldin, Carl-Henrik, Westermark, Bengt, Ohlsson, Rolf

Journal:

Year:

1985

Language:

english

File:

PDF, 25.34 MB

english, 1985

7

The gene for diffuse palmoplantar keratoderma of the type found in northern Sweden is localized to chromosome 12q11-q13

Lind, Lisbet, Lundström, Anita, Hofer, Per-Åke, Holmgren, Gösta

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 1.98 MB

english, 1994

8

Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia

Christine Klein, Nadia Gurvich, Miguel Sena-Esteves, Susan Bressman, Mitchell F. Brin, Barbara J. Ebersole, Stephen Fink, Lars Forsgren, Jennifer Friedman, David Grimes, Gosta Holmgren, Mårtin Kyllerm

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 6.55 MB

english, 2000

9

Second trimester prenatal diagnosis of the fragile X

Niels Tommerup, Pertti Aula, Björn Gustavii, Arvid Heiberg, Gösta Holmgren, Harriet von Koskull, Jaakko Leisti, Margareta Mikkelsen, Felix Mitelman, Karen B. Nielsen, Peter Steinbach, Sabine Stengel-R

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 603 KB

english, 1986

10

Infantile autism and the fragile X. A swedish multicenter study

Jan Wahlström, Christopher Gillberg, Karl-Henrik Gustavson, Gösta Holmgren, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 256 KB

english, 1986

11

Fragile X: Carrier detection in pregnancy

Niels Tommerup, Gösta Holmgren, Peter Steinbach, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 175 KB

english, 1986

12

Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county

Karl-Henrik Gustavson, Hans Blomquist K:son, Gösta Holmgren, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 268 KB

english, 1986

13

Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304

Niklas Dahl, Helena Malmgren, Ulf Pettersson, Gösta Holmgren, Eva Seemanová, Karl-Henrik Gustavson

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 275 KB

english, 1991

14

Fragile X families in a Northern Swedish County: A genealogical study of possibly affected individuals in the nineteenth century

Ulf Drugge, Hans K:son Blomquist, Karl-Henrik Gustavson, Gösta Holmgren

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 364 KB

english, 1991

15

Association of the Robin sequence with the fragile X syndrome

Ave M. Lachiewicz, Stanton F. Hoegerman, Gösta Holmgren, Eva Holmberg, Kristian Arinbjarnarson

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 469 KB

english, 1991

16

Methylation and mutation patterns in the fragile X syndrome

Helena Malmgren, Marie-Louise Steén-Bondeson, Karl-Henrik Gustavson, Eva Seémanova, Gösta Holmgren, Isabelle Oberlé, Jean-Louis Mandel, Ulf Pettersson, Niklas Dahl

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 749 KB

english, 1992

17

Gene therapy: Lessons learned from liver transplantation for transthyretin-amyloidosis

Ole B. Suhr, Gösta Holmgren, Erik Lundgren

Journal:

Liver Transplantation

Year:

2004

Language:

english

File:

PDF, 75 KB

english, 2004

18

Letters to the editor

Giuseppe Francesco Stefanini, Francesco Giuseppe Foschi, Lorenzo Marsigli, Cristiana Fumelli, Gian Luca Grazi, Gunnar Söderdahl, Ole Suhr, Professor Gösta Holmgren, Gustaf Herlenius, Bo-Göran Ericzon,

Journal:

Liver Transplantation

Year:

1996

Language:

english

File:

PDF, 370 KB

english, 1996

19

Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients

Carina Kärrman Mårdh, Birgitta Bäckman, Darrin Simmons, Irina Golovleva, Ting Ting Gu, Gösta Holmgren, Mary MacDougall, Kristina Forsman-Semb

Journal:

European Journal of Oral Sciences

Year:

2001

Language:

english

File:

PDF, 125 KB

english, 2001

20

Angioid streaks are part of a familial syndrome of dyserythropoietic anaemia (CDA III)

Herbert Sandström, Anders Wahlin, Mikael Eriksson, Gösta Holmgren, Lisbeth Lind, Ola Sandgren

Journal:

British Journal of Haematology

Year:

1997

Language:

english

File:

PDF, 491 KB

english, 1997

21

Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001

Erik Forestier, Sverre Heim, Elisabeth Blennow, Georg Borgström, Gösta Holmgren, Kristiina Heinonen, Johann Johannsson, Gitte Kerndrup, Mette Klarskov Andersen, Catarina Lundin, Ann Nordgren, Richard

Journal:

British Journal of Haematology

Year:

2003

Language:

english

File:

PDF, 567 KB

english, 2003

22

Peri- and paracentric inversions in chromosome 12: Prenatal diagnosis and family study

Hanne Poulsen, Margareta Mikkelsen, Gösta Holmgren

Journal:

Prenatal Diagnosis

Year:

1981

Language:

english

File:

PDF, 463 KB

english, 1981

23

Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia

Deborah Schuback, Patricia Kramer, Laurie Ozelius, Gösta Holmgren, Lars Forsgren, Marten Kyllerman, Jan Wahlström, Cheryl M. Craft, Torbjoern Nygaard, Mitchell Brin, Deborah Leon, Susan Bressman, Caro

Journal:

Year:

1991

Language:

english

File:

PDF, 679 KB

english, 1991

24

Haplotype analysis of common transthyretin mutations

Maria Rosário Almeida, N. Aoyama-Oishi, Yoshiyuki Sakaki, Gosta Holmgren, Drugge Ulf, Alessandra Ferlini, Fabrizio Salvi, Miguel Munar-Qués, Merrill D. Benson, Martha Skinner, Pedro P. Costa, Maria Jo

Journal:

Year:

1995

Language:

english

File:

PDF, 450 KB

english, 1995

25

Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids

Caroline Graff, Anna Eriksson, Kristina Forsman, Ola Sandgren, Gösta Holmgren, Claes Wadelius

Journal:

Year:

1997

Language:

english

File:

PDF, 113 KB

english, 1997

26

Transferrin Types in the Swedish Population

BECKMAN, LARS, HOLMGREN, GÖSTA, MÅRTENSSON, ERIK H.

Journal:

Year:

1962

File:

PDF, 255 KB

1962

27

10.1038/915

Petrukhin, Konstantin, Wadelius, Claes, Koisti, Markus J., Bakall, Benjamin, Li, Wen, Xie, Guochun, Marknell, Towa, Sandgren, Ola, Forsman, Kristina, Holmgren, Gösta, Andreasson, Sten, Vujic, Mihailo,

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 376 KB

english, 1998

28

Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia

Sun, Chen, Tranebjærg, Lisbeth, Torbergsen, Torberg, Holmgren, Gösta, Van Ghelue, Marijke

Journal:

European Journal of Human Genetics

Year:

2010

File:

PDF, 156 KB

2010

29

PMP22 Thr(118)Met: recessive CMT1 mutation or polymorphism?

Nelis, Eva, Holmberg, Bengt, Adolfsson, Rolf, Holmgren, Gösta, Broeckhoven, Christine Van

Journal:

Nature Genetics

Year:

1997

File:

PDF, 350 KB

1997

30

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia

Jonasson, Jenni, Juvonen, Vesa, Sistonen, Pertti, Ignatius, Jaakko, Johansson, Daniel, Björck, Erik J, Wahlström, Jan, Melberg, Atle, Holmgren, Gösta, Forsgren, Lars

Journal:

European Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 99 KB

english, 2000

31

Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia

Sun, Chen, Tranebjærg, Lisbeth, Torbergsen, Torberg, Holmgren, Gösta, Van Ghelue, Marijke

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 153 KB

english, 2001

32

The CTLA4 region as a general autoimmunity factor: An extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease

Einarsdottir, Elisabet, Söderström, Ingegerd, Löfgren-Burström, Anna, Haraldsson, Susann, Nilsson-Ardnor, Sofie, Penha-Goncalves, Carlos, Lind, Lisbet, Holmgren, Gösta, Holmberg, Monica, Asplund, Kjel

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 93 KB

english, 2003

33

Haplotypes and DNA sequence variation within and surrounding the transthyretin gene: genotype–phenotype correlations in familial amyloid polyneuropathy (V30M) in Portugal and Sweden

Soares, Miguel Luz, Coelho, Teresa, Sousa, Alda, Holmgren, Gösta, Saraiva, Maria João, Kastner, Daniel L, Buxbaum, Joel N

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 226 KB

english, 2003

34

Genetic heterogeneity of autosomal dominant amelogenesis imperfecta demonstrated by its exclusion from the AIH2 region on human chromosome 4Q

Carina Kärrman, Birgitta Bäckman, Gösta Holmgren, Kristina Forsman

Journal:

Archives of Oral Biology

Year:

1996

Language:

english

File:

PDF, 646 KB

english, 1996

35

Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping

Ann Nordgren, Filip Farnebo, Bertil Johansson, Gösta Holmgren, Erik Forestier, Catharina Larsson, Stefan Söderhäll, Magnus Nordenskjöld, Elisabeth Blennow

Journal:

European Journal of Haematology

Year:

2001

Language:

english

File:

PDF, 380 KB

english, 2001

36

Le BCG administré par des injections intraveineuses

I. HOLMGREN, GÖSTA LJUNGBERG

Journal:

Journal of Internal Medicine

Year:

1935

Language:

french

File:

PDF, 405 KB

french, 1935

37

Hyperaminoaciduria in Mild Phosphate Diabetes in Adults

Gösta Holmgren, Bengt Lindqvist, Erik Lundberg

Journal:

Journal of Internal Medicine

Year:

1980

Language:

english

File:

PDF, 198 KB

english, 1980

38

Congenital Dyserythropoietic Anaemia Type III: an Electron Microscopic Study

Bengt Björkstén, Gösta Holmgren, Göran Roos And, Roger Stenling

Journal:

British Journal of Haematology

Year:

1978

Language:

english

File:

PDF, 968 KB

english, 1978

39

Heart Transplantation in a 68-Year-Old Patient with Senile Systemic Amyloidosis

Uwe Fuchs, Armin Zittermann, Ole Suhr, Gösta Holmgren, Gero Tenderich, Kazutomo Minami, Reiner Koerfer

Journal:

American Journal of Transplantation

Year:

2005

Language:

english

File:

PDF, 72 KB

english, 2005

40

IMMUNODIFFUSION STUDIES ON ESCHERICHIA COLI : 1. Identification of O, K and H Antigens in an O6 Strain

Jan Holmgren, Gösta Eggertsen, LarsÅ. Hanson, Knut Lincoln

Journal:

Year:

1969

Language:

english

File:

PDF, 854 KB

english, 1969

41

Effect of folic acid treatment in the fragile X syndrome

Karl-Henrik Gustavson, Kate Dahlbom, Anders Flood, Gösta Holmgren, Hans K→son Blomquist, Gunnar Sanner

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 294 KB

english, 1985

42

Lethal and non-lethal diastrophic dysplasia A study of 14 Swedish cases

Karl-Henrik Gustavson, Gösta Holmgren, Sten Jagell, Håkan Jorulf

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 894 KB

english, 1985

43

Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis

Gösta Holmgren, Eva Holmberg, Anita Lindström, Eleonor Lindström, Ingrid Nordenson, Ola Sandgren, Lars Steen, Birgitta Svensson, Erik Lundgren, Alex von Gabain

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 360 KB

english, 1988

44

Multiplex PCR excludes Duchenne muscular dystrophy in a twin pregnancy

Claes Wadelius, Göran Annéren, Niklas Dahl, Gösta Holmgren, Karl-Henrik Gustavson

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 189 KB

english, 1991

45

Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30)

Gösta Holmgren, Lars Steen, Jan Ekstedt, Carl-Gustav Groth, B.-G. Ericzon, Siv Eriksson, Oluf Andersen, Ingvar Karlberg, Gunnela Nordén, Masamitsu Nakazato, Philip Hawkins, Suzanne Richardson, Mark Pe

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 336 KB

english, 1991

46

The gene for Best's macular dystrophy is located at 11q13 in a Swedish family

Kristina Forsman, Caroline Graff, Stefan Nordström, Kent Johansson, Eleonora Westermark, Erik Lundgren, Karl-Henrik Gustavson, Claes Wadelius, Gösta Holmgren

Journal:

Clinical Genetics

Year:

1992

Language:

english

File:

PDF, 392 KB

english, 1992

47

Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences

Gōsta Holmgren, Sven Bergström, Ulf Drugge, Erik Lundgren, Carin Nording-Sikström, Ola Sandgren, Lars Steen

Journal:

Clinical Genetics

Year:

1992

Language:

english

File:

PDF, 311 KB

english, 1992

48

Glycerol kinase deficiency in two brothers with and without clinical manifestations

Hans K:son Blomquist, Niklas Dahl, Lars Gustafsson, Christina Heilerud, Elisabeth Holme, Gösta Holmgren, Lars Matsson, Monika von Zweigbergk

Journal:

Clinical Genetics

Year:

1996

Language:

english

File:

PDF, 673 KB

english, 1996

49

A New Simple and Rapid Screening Method for Variant Transthyretin-Related Amyloidosis

Yukio Ando, Per-Ingvar Ohlsson, Ole Suhr, Nils Nyhlin, Taro Yamashita, Gösta Holmgren, Åke Danielsson, Ola Sandgren, Makoto Uchino, Masayuki Ando

Journal:

Biochemical and Biophysical Research Communications

Year:

1996

Language:

english

File:

PDF, 65 KB

english, 1996

50

Oxidative Stress Is Found in Amyloid Deposits in Systemic Amyloidosis

Yukio Ando, Nils Nyhlin, Ole Suhr, Gösta Holmgren, Koji Uchida, Magdy El Sahly, Taro Yamashita, Hisayasu Terasaki, Masaaki Nakamura, Makoto Uchino, Masayuki Ando

Journal:

Biochemical and Biophysical Research Communications

Year:

1997

Language:

english

File:

PDF, 557 KB

english, 1997