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Lars Hagenfeldt

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Sweden

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TOP 3
Ann Gardner; Anna Johansson; Rolf Wibom; Inger Nennesmo; Ulrika von Döbeln; Lars Hagenfeldt; Tore Hällström
Alterations of mitochondrial function and correlations with personality traits in selected major depressive disorder patients.
Rolf Wibom; Lars Hagenfeldt; Ulrika von Döbeln
Measurement of ATP production and respiratory chain enzyme activities in mitochondria isolated from small muscle biopsy samples.
Anna Nordenström; Anna Wedell; Lars Hagenfeldt; Claude Marcus; Agne Larsson
Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infants.

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All Publications

2003: Ann Gardner; Anna Johansson; Rolf Wibom; Inger Nennesmo; Ulrika von Döbeln; Lars Hagenfeldt; Tore Hällström
Alterations of mitochondrial function and correlations with personality traits in selected major depressive disorder patients.
Journal of affective disorders 2003;76(1-3):55-68.
2002: Rolf Wibom; Lars Hagenfeldt; Ulrika von Döbeln
Measurement of ATP production and respiratory chain enzyme activities in mitochondria isolated from small muscle biopsy samples.
Analytical biochemistry 2002;311(2):139-51.
2001: Anna Nordenström; Anna Wedell; Lars Hagenfeldt; Claude Marcus; Agne Larsson
Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infants.
Pediatrics 2001;108(4):E68.
2001: Lena Flyckt; Nikolaos Venizelos; Gunnar Edman; Lars Bjerkenstedt; Lars Hagenfeldt; Frits-Axel Wiesel
Aberrant tyrosine transport across the cell membrane in patients with schizophrenia.
Archives of general psychiatry 2001;58(10):953-8.
2001: Drude Fugelseth; Claes Guthenberg; Lars Hagenfeldt; Knut Liestøl; M Hallerud; Rolf Lindemann
Patent ductus venosus does not lead to alimentary galactosaemia in preterm infants.
Acta paediatrica (Oslo, Norway : 1992) 2001;90(2):192-5.
1999: Frits-Axel Wiesel; Jesper L R Andersson; G Westerberg; IM Wieselgren; Lars Bjerkenstedt; Lars Hagenfeldt; Bengt Långström
Tyrosine transport is regulated differently in patients with schizophrenia.
Schizophrenia research 1999;40(1):37-42.
1999: EL Appelkvist; Nikolaos Venizelos; Y Zhang; Ingela Parmryd; Lars Hagenfeldt; Gustav Dallner
Synthesis of mevalonate pathway lipids in fibroblasts from Zellweger and X-linked ALD patients.
Pediatric research 1999;46(3):345-50.
1999: A Johansson; Claes Guthenberg; H Ahlman; Ulrika von Döbeln; Lars Hagenfeldt
Prevalence of the 985A>G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Sweden.
Scandinavian journal of clinical and laboratory investigation 1999;59(4):289-91.
1999: Anna Nordenström; A Thilén; Lars Hagenfeldt; Agne Larsson; Anna Wedell
Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
The Journal of clinical endocrinology and metabolism 1999;84(5):1505-9.
1998: G Solders; G Celsing; Lars Hagenfeldt; P Ljungman; B Isberg; O Ringdén
Improved peripheral nerve conduction, EEG and verbal IQ after bone marrow transplantation for adult metachromatic leukodystrophy.
Bone marrow transplantation 1998;22(11):1119-22.
1998: Nikolaos Venizelos; Ulrika von Döbeln; Lars Hagenfeldt
Fatty acid oxidation in fibroblasts from patients with defects in beta-oxidation and in the respiratory chain.
Journal of inherited metabolic disease 1998;21(4):409-15.
1998: A Thil'en; Anna Nordenström; Lars Hagenfeldt; Ulrika von Döbeln; Claes Guthenberg; Agne Larsson
Benefits of neonatal screening for congenital adrenal hyperplasia (21-hydroxylase deficiency) in Sweden.
Pediatrics 1998;101(4):E11.
1997: BA Larsson; A Nörstmo; Claes Guthenberg; Gunnar L Olsson; P Danielsson; Lars Hagenfeldt; G Elander; A Larsson
[The routine sampling procedure for PKU should be changed. Venous puncture is less painful than heel lancing].
Läkartidningen 1997;94(49):4625-8.
1997: Gunilla Malm; O Ringdén; M Anvret; Ulrika von Döbeln; Lars Hagenfeldt; B Isberg; S Knuutila; I Nennesmo; Jacek Winiarski; Claude Marcus
Treatment of adrenoleukodystrophy with bone marrow transplantation.
Acta paediatrica (Oslo, Norway : 1992) 1997;86(5):484-92.
1995: Lars Hagenfeldt; Nikolaos Venizelos; Ulrika von Döbeln
Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease 1995;18(2):245-8.
1994: Nikolaos Venizelos; L Ijlst; R J Wanders; Lars Hagenfeldt
beta-Oxidation enzymes in fibroblasts from patients with 3-hydroxydicarboxylic aciduria.
Pediatric research 1994;36(1 Pt 1):111-4.
1994: E Svensson; L Iselius; Lars Hagenfeldt
Severity of mutation in the phenylalanine hydroxylase gene influences phenylalanine metabolism in phenylketonuria and hyperphenylalaninaemia heterozygotes.
Journal of inherited metabolic disease 1994;17(2):215-22.
1994: Ulrika von Döbeln; Nikolaos Venizelos; M Westgren; Lars Hagenfeldt
Long-chain 3-hydroxyacyl-CoA dehydrogenase in chorionic villi, fetal liver and fibroblasts and prenatal diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease 1994;17(2):185-8.
1993: Ulrika von Döbeln; R Wibom; H Ahlman; I Nennesmo; H Nyctelius; Eric Hultman; Lars Hagenfeldt
Fatal neonatal lactic acidosis with respiratory insufficiency due to complex I and IV deficiency.
Acta paediatrica (Oslo, Norway : 1992) 1993;82(12):1079-81.
1993: E Svensson; Ulrika von Döbeln; Randy C Eisensmith; Lars Hagenfeldt; SL Woo
Relation between genotype and phenotype in Swedish phenylketonuria and hyperphenylalaninemia patients.
European journal of pediatrics 1993;152(2):132-9.
1993: E Svensson; Y Wang; Randy C Eisensmith; Lars Hagenfeldt; SL Woo
Three polymorphisms but no disease-causing mutations in the proximal part of the promoter of the phenylalanine hydroxylase gene.
European journal of human genetics : EJHG 1993;1(4):306-13.
1992: E Svensson; Randy C Eisensmith; B Dworniczak; Ulrika von Döbeln; Lars Hagenfeldt; J Horst; SL Woo
Two missense mutations causing mild hyperphenylalaninemia associated with DNA haplotype 12.
Human mutation 1992;1(2):129-37.
1991: E Svensson; Ulrika von Döbeln; Lars Hagenfeldt
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families.
Human genetics 1991;87(1):11-7.
1990: E Svensson; B Andersson; Lars Hagenfeldt
Two mutations within the coding sequence of the phenylalanine hydroxylase gene.
Human genetics 1990;85(3):300-4.
1990: Lars Hagenfeldt; Ulrika von Döbeln; E Holme; J Alm; G Brandberg; E Enocksson; L Lindeberg
3-Hydroxydicarboxylic aciduria--a fatty acid oxidation defect with severe prognosis.
The Journal of pediatrics 1990;116(3):387-92.
1990: Ulrika von Döbeln; Nikolaos Venizelos; Lars Hagenfeldt
Retrospective diagnosis of 3-hydroxydicarboxylic aciduria by analysis of filter paper blood samples.
Journal of inherited metabolic disease 1990;13(2):165-8.
1988: A Larsson; Lars Hagenfeldt; Ulrika von Döbeln; T Curstedt; J Gustafsson; E Svensson
Neonatal screening for congenital adrenal hyperplasia using 17-hydroxyprogesterone assay in filter paper blood spots.
Hormone research 1988;30(6):235-40.
1987: Lars Hagenfeldt; Nikolaos Venizelos; Lars Bjerkenstedt; F A Wiesel
Decreased tyrosine transport in fibroblasts from schizophrenic patients.
Life sciences 1987;41(25):2749-57.
1987: Lars Hagenfeldt; I Bollgren; Nikolaos Venizelos
N-acetylaspartic aciduria due to aspartoacylase deficiency--a new aetiology of childhood leukodystrophy.
Journal of inherited metabolic disease 1987;10(2):135-41.