List of works - Gosta Holmgren

A Swedish family with the rare Phe33Leu transthyretin mutation

scientific article published in September 2005

A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception

scientific article

A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).

scientific article

Apolipoprotein E4 genotype is not a risk factor for systemic AA amyloidosis or familial amyloid polyneuropathy

Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.

scientific article

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

scientific article published in May 2003

Difficulties in clinical diagnosis and prediction of outcome in patients with the transthyretin Met 30 mutation: Report of two cases

Discordant symptoms in monozygotic twins with familial amyloidotic polyneuropathy (FAP) (TTR Met 30)

Disease-causing mutations in the cellular retinaldehyde binding protein tighten and abolish ligand interactions

scientific article (publication date: 4 April 2003)

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

scientific article

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

scientific article published in March 2004

Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser

article

Heart transplantation in a 68-year-old patient with senile systemic amyloidosis

scientific article published in May 2005

L-threo-DOPS treatment of orthostatic hypotension in Swedish patients with familial amyloidotic polyneuropathy (TTR-met30)

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

scientific article published on 14 January 2010

Successful pregnancies and fatherhood in familial amyloidotic polyneuropathy (FAP Val30Met) patients with liver transplantation

scientific article published in June 2004

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

article

Transthyretin Ser6 as a neutral polymorphism in familial amyloidotic polyneuropathy

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

scientific article published on December 1, 1991

List of works by Gosta Holmgren

A Swedish family with the rare Phe33Leu transthyretin mutation

A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception

A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).

Apolipoprotein E4 genotype is not a risk factor for systemic AA amyloidosis or familial amyloid polyneuropathy

Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.

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

Difficulties in clinical diagnosis and prediction of outcome in patients with the transthyretin Met 30 mutation: Report of two cases

Discordant symptoms in monozygotic twins with familial amyloidotic polyneuropathy (FAP) (TTR Met 30)

Disease-causing mutations in the cellular retinaldehyde binding protein tighten and abolish ligand interactions

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

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

Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser

Heart transplantation in a 68-year-old patient with senile systemic amyloidosis

L-threo-DOPS treatment of orthostatic hypotension in Swedish patients with familial amyloidotic polyneuropathy (TTR-met30)

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

Successful pregnancies and fatherhood in familial amyloidotic polyneuropathy (FAP Val30Met) patients with liver transplantation

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

Transthyretin Ser6 as a neutral polymorphism in familial amyloidotic polyneuropathy

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

World-wide survey of liver transplantation in patients with familial amyloidotic polyneuropathy