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Longitudinal Smartphone-Based Post-hospitalisation Symptom Monitoring in SARS-CoV-2 Associated Respiratory Failure: A Multi-Centre Observational Study

Frontiers in rehabilitation sciences, 2021-11, Vol.2, p.777396-777396

2021

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Variegate Porphyria in Western Europe: Identification of PPOX Gene Mutations in 104 Families, Extent of Allelic Heterogeneity, and Absence of Correlation between Phenotype and Type of Mutation

American journal of human genetics, 1999-10, Vol.65 (4), p.984-994

1999

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Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms

Human molecular genetics, 1994-03, Vol.3 (3), p.477-480

1994

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Erythropoietic protoporphyria and hepatic complications

Journal of hepatology, 1992, Vol.16 (1), p.4-6

Nordmann, Yves

1992

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A Telemonitoring and Hybrid Virtual Coaching Solution “CAir” for Patients with Chronic Obstructive Pulmonary Disease: Protocol for a Randomized Controlled Trial

JMIR research protocols, 2020-10, Vol.9 (10), p.e20412-e20412

2020

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Human hereditary hepatic porphyrias

Clinica Chimica Acta, 2002-11, Vol.325 (1), p.17-37

2002

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Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene

Biochemical and biophysical research communications, 1991-12, Vol.181 (2), p.594-599

1991

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Three novel mutations in the coproporphyrinogen oxidase gene

Human mutation, 1997, Vol.9 (1), p.78-80

1997

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Ferrochelatase Structural Mutant ( Fech m1Pas) in the House Mouse

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.645-648

1993

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Porphyries érythropoïétiques

EMC - Hématologie, 2006-01, Vol.1 (1), p.1-5

Nordmann, Yves

2006

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Improving body composition and physical activity in Prader-Willi Syndrome

The Journal of pediatrics, 2003-01, Vol.142 (1), p.73-78

2003

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Sterbehilfe aus der Sicht der jüdischen Medizinethik

Handbuch Sterben und Menschenwürde, 2012, p.307-316

2012

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Hepatocellular carcinoma in patients with acute hepatic porphyria: frequency of occurrence and related factors

Journal of hepatology, 2000-06, Vol.32 (6), p.933-939

2000

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Inheritance in Erythropoietic Protoporphyria: A Common Wild-Type Ferrochelatase Allelic Variant With Low Expression Accounts for Clinical Manifestation

Blood, 1999-03, Vol.93 (6), p.2105-2110

1999

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HOMOZYGOUS CASE OF HEREDITARY COPROPORPHYRIA

The Lancet (British edition), 1977-12, Vol.310 (8052), p.1348-1349

1977

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Sudden death of an infant with Prader-Willi syndrome: Not a unique case?

Biology of the neonate, 2002-01, Vol.82 (2), p.139-141

2002

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Breathing New Life into COPD Assessment: Multisensory Home-monitoring for Predicting Severity

Proceedings of the 25th International Conference on Multimodal Interaction, 2023, p.84-93

2023

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Der Beginn menschlichen Lebens: Aus Sicht der jüdischen Bioethik

RU : Ökumenische Zeitschrift für den Religionsunterricht, 2003, Vol.33 (3), p.92-93

Nordmann, Yves

2003

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Fatal Outcome of Sleep Apnoea in PWS during the Initial Phase of Growth Hormone Treatment

Hormone research in paediatrics, 2002-03, Vol.58 (Suppl. 3), p.24-26

2002

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EFFECT OF GLUTEN‐CONTAINING DIET ON SERUM ZONULIN AND INTESTINAL PERMEABILITY IN TYPE 1 DIABETES CHILDREN AND THEIR RELATIVES

Journal of pediatric gastroenterology and nutrition, 2005-10, Vol.41 (4), p.558-558

2005

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Heme and acute inflammation

European journal of biochemistry, 1999-03, Vol.261 (1), p.190-196

1999

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Early manifestations of Prader-Willi syndrome: influence of growth hormone

Journal of pediatric endocrinology & metabolism : JPEM, 2001, Vol.14 Suppl 6, p.1441

2001

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Epidemiology of hepatitis C and G in sporadic and familial porphyria cutanea tarda

Hepatology (Baltimore, Md.), 1998-03, Vol.27 (3), p.848-852

1998

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Molecular characterization of homozygous variegate porphyria

Human molecular genetics, 1998-11, Vol.7 (12), p.1921-1925

1998

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Correction of congenital erythropoietic porphyria by bone marrow transplantation

The Journal of pediatrics, 1996-09, Vol.129 (3), p.453-456

1996

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Longitudinal Smartphone-Based Post-hospitalisation Symptom Monitoring in SARS-CoV-2 Associated Respiratory Failure: A Multi-Centre Observational Study

Variegate Porphyria in Western Europe: Identification of PPOX Gene Mutations in 104 Families, Extent of Allelic Heterogeneity, and Absence of Correlation between Phenotype and Type of Mutation

Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms

Erythropoietic protoporphyria and hepatic complications

A Telemonitoring and Hybrid Virtual Coaching Solution “CAir” for Patients with Chronic Obstructive Pulmonary Disease: Protocol for a Randomized Controlled Trial

Human hereditary hepatic porphyrias

Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene

Three novel mutations in the coproporphyrinogen oxidase gene

Ferrochelatase Structural Mutant ( Fech m1Pas) in the House Mouse

Porphyries érythropoïétiques

Improving body composition and physical activity in Prader-Willi Syndrome

Sterbehilfe aus der Sicht der jüdischen Medizinethik

Hepatocellular carcinoma in patients with acute hepatic porphyria: frequency of occurrence and related factors

Inheritance in Erythropoietic Protoporphyria: A Common Wild-Type Ferrochelatase Allelic Variant With Low Expression Accounts for Clinical Manifestation

HOMOZYGOUS CASE OF HEREDITARY COPROPORPHYRIA

Sudden death of an infant with Prader-Willi syndrome: Not a unique case?

Breathing New Life into COPD Assessment: Multisensory Home-monitoring for Predicting Severity

Der Beginn menschlichen Lebens: Aus Sicht der jüdischen Bioethik

Fatal Outcome of Sleep Apnoea in PWS during the Initial Phase of Growth Hormone Treatment

EFFECT OF GLUTEN‐CONTAINING DIET ON SERUM ZONULIN AND INTESTINAL PERMEABILITY IN TYPE 1 DIABETES CHILDREN AND THEIR RELATIVES

Heme and acute inflammation

Early manifestations of Prader-Willi syndrome: influence of growth hormone

Epidemiology of hepatitis C and G in sporadic and familial porphyria cutanea tarda

Molecular characterization of homozygous variegate porphyria

Correction of congenital erythropoietic porphyria by bone marrow transplantation

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