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High mortality rates among GHB abusers in Western Sweden

Clinical toxicology (Philadelphia, Pa.), 2008-03, Vol.46 (3), p.187-192

2008

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Hepatocellular carcinoma despite long‐term survival in chronic tyrosinaemia I

Journal of inherited metabolic disease, 2000-12, Vol.23 (8), p.791-804

2000

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Partial epilepsy in a girl with a symptom‐free sister: First two Finnish patients with dihydropyrimidine dehydrogenase deficiency

Journal of inherited metabolic disease, 1997-09, Vol.20 (5), p.719-720

1997

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Urinary organic acids: isolation and quantification for routine metabolic screening

Clinical chemistry (Baltimore, Md.), 1987-04, Vol.33 (4), p.473-480

1987

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Pyruvate‐Carboxylase Deficiency with Urea Cycle Impairment

Acta Paediatrica, 1985-11, Vol.74 (6), p.982-986

1985

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3-hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis

Clinical chemistry (Baltimore, Md.), 1980-02, Vol.26 (2), p.261-265

1980

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Carnitine deficiency induced by pivampicillin and pivmecillinam therapy

The Lancet (British edition), 1989-08, Vol.2 (8661), p.469

1989

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CARNITINE DEFICIENCY INDUCED BY PIVAMPICILLIN AND PIVMECILLINAM THERAPY

The Lancet (British edition), 1989-08, Vol.334 (8661), p.469-473

1989

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2,6-Dimethyloctanedioic acid--a metabolite of phytanic acid in Refsum's disease

Clinical chemistry (Baltimore, Md.), 1983-03, Vol.29 (3), p.434-437

1983

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Urinary metabolites of cis-9,10-methylene octadecanoic acid. cis-3,4-Methylene hexanedioic acid and related compounds

The Journal of biological chemistry, 1979-04, Vol.254 (8), p.2807-2813

1979

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Biotin‐responsive 3‐methylcrotonylglycinuria with biotinidase deficiency

Journal of inherited metabolic disease, 1985-06, Vol.8 (S2), p.103-104

1985

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Treatment of hereditary tyrosinaemia (fumarylacetoacetase deficiency) by enzyme substitution

Journal of inherited metabolic disease, 1986-06, Vol.9 (S2), p.257-261

1986

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Urinary excretion of thymine and uracil in a two-year-old child with a malignant tumor of the brain

Clinical chemistry (Baltimore, Md.), 1979-07, Vol.25 (7), p.1325-1328

1979

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Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria

Pediatric research, 1992-12, Vol.32 (6), p.731-735

1992

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Volkstümliches aus Rotenburg (Luzern)

Schweizerisches Archiv für Volkskunde, 1935-01, Vol.34 (1), p.28

Greter, J

1935

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Réinventer l'école? Politiques, conceptions et pratiques dites inclusives

Institut National Supérieur de Formation et de Recherche pour l'Éducation des Jeunes Handicapés et les Enseignements Adaptés (Suresnes)

2016

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Septumless injection port for capillary gas chromatography

Analytical chemistry (Washington), 1982-08, Vol.54 (9), p.1646-1647

1982

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2-Hydroxy-2-methylsuccinic acid — a urinary metabolite in propionyl-CoA carboxylase deficiency

Clinica chimica acta, 1980-01, Vol.106 (1), p.103-106

1980

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High-Dimensional Single-Cell Mapping of Central Nervous System Immune Cells Reveals Distinct Myeloid Subsets in Health, Aging, and Disease

Immunity (Cambridge, Mass.), 2018-02, Vol.48 (2), p.380-395.e6

2018

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3-hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis

Clinical chemistry (Baltimore, Md.), 1980-02, Vol.26 (2), p.261-265

1980

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Bhlhe40 and Bhlhe41 transcription factors regulate alveolar macrophage self‐renewal and identity

The EMBO journal, 2019-10, Vol.38 (19), p.e101233-n/a

2019

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GM-CSF Controls Nonlymphoid Tissue Dendritic Cell Homeostasis but Is Dispensable for the Differentiation of Inflammatory Dendritic Cells

Immunity (Cambridge, Mass.), 2012-06, Vol.36 (6), p.1031-1046

2012

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The Cytokine GM-CSF Drives the Inflammatory Signature of CCR2+ Monocytes and Licenses Autoimmunity

Immunity (Cambridge, Mass.), 2015-09, Vol.43 (3), p.502-514

2015

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3-methylglutaconic aciduria: report on a sibship with infantile progressive encephalopathy

European journal of pediatrics, 1978-12, Vol.129 (4), p.231-238

1978

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High mortality rates among GHB abusers in Western Sweden

Hepatocellular carcinoma despite long‐term survival in chronic tyrosinaemia I

Partial epilepsy in a girl with a symptom‐free sister: First two Finnish patients with dihydropyrimidine dehydrogenase deficiency

Urinary organic acids: isolation and quantification for routine metabolic screening

Pyruvate‐Carboxylase Deficiency with Urea Cycle Impairment

3-hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis

Carnitine deficiency induced by pivampicillin and pivmecillinam therapy

CARNITINE DEFICIENCY INDUCED BY PIVAMPICILLIN AND PIVMECILLINAM THERAPY

2,6-Dimethyloctanedioic acid--a metabolite of phytanic acid in Refsum's disease

Urinary metabolites of cis-9,10-methylene octadecanoic acid. cis-3,4-Methylene hexanedioic acid and related compounds

Biotin‐responsive 3‐methylcrotonylglycinuria with biotinidase deficiency

Treatment of hereditary tyrosinaemia (fumarylacetoacetase deficiency) by enzyme substitution

Urinary excretion of thymine and uracil in a two-year-old child with a malignant tumor of the brain

Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria

Volkstümliches aus Rotenburg (Luzern)

Réinventer l'école? Politiques, conceptions et pratiques dites inclusives

Septumless injection port for capillary gas chromatography

2-Hydroxy-2-methylsuccinic acid — a urinary metabolite in propionyl-CoA carboxylase deficiency

High-Dimensional Single-Cell Mapping of Central Nervous System Immune Cells Reveals Distinct Myeloid Subsets in Health, Aging, and Disease

3-hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis

Bhlhe40 and Bhlhe41 transcription factors regulate alveolar macrophage self‐renewal and identity

GM-CSF Controls Nonlymphoid Tissue Dendritic Cell Homeostasis but Is Dispensable for the Differentiation of Inflammatory Dendritic Cells

Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific Manner

The Cytokine GM-CSF Drives the Inflammatory Signature of CCR2+ Monocytes and Licenses Autoimmunity

3-methylglutaconic aciduria: report on a sibship with infantile progressive encephalopathy

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