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Troponin as a risk factor for mortality in critically ill patients without acute coronary syndromes

Journal of the American College of Cardiology, 2003-06, Vol.41 (11), p.2004-2009

2003

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Lack of Effect of Oral Charcoal in Congenital Erythropoietic Porphyria

The New England journal of medicine, 1994-04, Vol.330 (15), p.1092-1094

1994

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Systematic Analysis of Molecular Defects in the Ferrochelatase Gene from Patients with Erythropoietic Protoporphyria

American journal of human genetics, 1998-06, Vol.62 (6), p.1341-1352

1998

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Influence of age and gender on the clinical expression of acute intermittent porphyria based on molecular study of porphobilinogen deaminase gene among Swiss patients

Molecular medicine (Cambridge, Mass.), 2001-08, Vol.7 (8), p.535-542

2001

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Nine novel mutations in the hydroxymethylbilane synthase gene of Polish patients with acute intermittent porphyria

Clinical genetics, 2006-03, Vol.69 (3), p.284-286

2006

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A “null allele” mutation is responsible for erythropoietic protoporphyria in an Israeli patient who underwent liver transplantation: relationships among biochemical, clinical, and genetic parameters

Blood cells, molecules, & diseases, 2003-05, Vol.30 (3), p.298-301

2003

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Development of a gas chromatography-mass spectrometry method for determination of ketamine in plasma and its application to human samples

Therapeutic drug monitoring, 1995-02, Vol.17 (1), p.95-100

1995

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Molecular defects in erythropoietic protoporphyria with terminal liver failure

Human genetics, 1994-06, Vol.93 (6), p.711-713

1994

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Human ferrochelatase : a novel mutation in patients with erythropoietic protoporphyria and an isoform caused by alternative splicing

Human genetics, 1995-04, Vol.95 (4), p.391-396

1995

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Cytofluorometry as a Diagnosis of Protoporphyria

Gastroenterology (New York, N.Y. 1943), 1992-03, Vol.102 (3), p.1044-1048

1992

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Radioimmunological determination of serum 3 beta-hydroxy-5-cholenoic acid in normal subjects and patients with liver disease

Journal of lipid research, 1979-11, Vol.20 (8), p.986-993

1979

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Polycythemia, polyglobulia and neurologic symptoms. Review based on 5 personal cases

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 1971-04, Vol.60 (15), p.465

Minder-von Goumoëns, I

1971

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Polycythemia, polyglobulia and neurologic symptoms. Review based on 5 personal cases

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 1971-04, Vol.60 (14), p.423

Minder-von Goumoëns, I

1971

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Labetalol: a field study in essential hypertension (author's transl)

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 1982-02, Vol.71 (8), p.332

1982

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Results of cardioversion in arrhythmias

Schweizerische medizinische Wochenschrift, 1969-10, Vol.99 (43), p.1546

1969

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Symptoms of functional disorders--epidemiologic research on the masticatory system of recruits (1974 and 1985)

Schweizer Monatsschrift fur Zahnmedizin = Revue mensuelle suisse d'odonto-stomatologie = Rivista mensile svizzera di odontologia e stomatologia, 1988, Vol.98 (11), p.1185

1988

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Troponin as a risk factor for mortality in critically ill patients without acute coronary syndromes

Lack of Effect of Oral Charcoal in Congenital Erythropoietic Porphyria

Systematic Analysis of Molecular Defects in the Ferrochelatase Gene from Patients with Erythropoietic Protoporphyria

Influence of age and gender on the clinical expression of acute intermittent porphyria based on molecular study of porphobilinogen deaminase gene among Swiss patients

Nine novel mutations in the hydroxymethylbilane synthase gene of Polish patients with acute intermittent porphyria

A “null allele” mutation is responsible for erythropoietic protoporphyria in an Israeli patient who underwent liver transplantation: relationships among biochemical, clinical, and genetic parameters

Development of a gas chromatography-mass spectrometry method for determination of ketamine in plasma and its application to human samples

Molecular defects in erythropoietic protoporphyria with terminal liver failure

Human ferrochelatase : a novel mutation in patients with erythropoietic protoporphyria and an isoform caused by alternative splicing

Cytofluorometry as a Diagnosis of Protoporphyria

Radioimmunological determination of serum 3 beta-hydroxy-5-cholenoic acid in normal subjects and patients with liver disease

Polycythemia, polyglobulia and neurologic symptoms. Review based on 5 personal cases

Polycythemia, polyglobulia and neurologic symptoms. Review based on 5 personal cases

Labetalol: a field study in essential hypertension (author's transl)

Results of cardioversion in arrhythmias

Symptoms of functional disorders--epidemiologic research on the masticatory system of recruits (1974 and 1985)

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