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Balint's syndrome revealing Creutzfeldt-Jakob disease

Revue neurologique, 2022-03, Vol.178 (3), p.278-280

2022

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Interprofessional recommendations on behalf of Société française de radiothérapie oncologique for the prevention, protection and management of cyberattacks in radiation oncology

Cancer radiothérapie, 2023-12, Vol.27 (8), p.683-688

2023

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Prévention, protection, et gestion des cyberattaques en oncologie radiothérapie : recommandations interprofessionnelles au nom de la Société française de radiothérapie oncologique

Cancer radiothérapie, 2023-12, Vol.27 (8), p.683-688

2023

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Radiothérapie externe du sein et des aires ganglionnaires : étude dosimétrique multicentrique

Cancer radiothérapie, 2018-10, Vol.22 (6-7), p.714-714

2018

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Dosimetric Evaluation of Modulated ArcTherapy (DEMAT)

Physica medica, 2015-11, Vol.31, p.e28-e29

2015

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22- A multi-center study of breast irradiation techniques

Physica medica, 2019-12, Vol.68, p.13-15

2019

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14 - Dosimetric Evaluation of Modulated ArcTherapy (DEMAT)

Physica medica, 2015-11, Vol.31, p.e28-e29

2015

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Clinical aspects and usefulness of indirect absorbed immunofluorescence for diagnosis of yaws in Central Africa

Journal of Clinical Microbiology, 1988-11, Vol.26 (11), p.2432-2433

1988

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Anti-(human LFA-1) monoclonal antibodies bind P815 murine tumour cells

Cancer Immunology Immunotherapy, 1992-11, Vol.34 (6), p.407-413

1992

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Analysis of the Gc polymorphism in human populations by isoelectrofocusing on polyacrylamide gels. Demonstration of subtypes of the Gc allele and of additional Gc variants

Human genetics, 1978-02, Vol.41 (1), p.53-60

1978

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The health of Central African students at the time of their arrival in France

Bulletin de la Societe de pathologie exotique et de ses filiales, 1975-11, Vol.68 (6), p.593

1975

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Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

British journal of dermatology (1951), 2020-10, Vol.183 (4), p.614-627

2020

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Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines

British journal of dermatology (1951), 2016-01, Vol.174 (1), p.56-67

2016

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Diagnosis and management of pemphigus: Recommendations of an international panel of experts

Journal of the American Academy of Dermatology, 2020-03, Vol.82 (3), p.575-585.e1

2020

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550 Daclatasvir improves life quality in murine recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2024-08, Vol.144 (8), p.S96-S96

2024

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Analysis of the Gc polymorphism in human populations by isoelectrofocusing on polyacrylamide gels. Demonstration of subtypes of the Gc1 allele and of additional Gc variants

Human genetics, 1978, Vol.41 (1)

1978

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Patients suffering from dystrophic epidermolysis bullosa are prone to developing autoantibodies against skin proteins: A longitudinal confirmational study

Experimental dermatology, 2024-02, Vol.33 (2), p.e15035-n/a

2024

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Gc, Tf, Hp subtype and alpha 1-antitrypsin polymorphisms in a Pygmy Bi-Aka sample

Human heredity, 1981, Vol.31 (3), p.129

1981

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Molecular epidemiology of junctional epidermolysis bullosa: discovery of novel and frequent LAMB3 mutations in Chilean patients with diagnostic significance

British journal of dermatology (1951), 2017-04, Vol.176 (4), p.1090-1092

2017

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Epidermolysis bullosa simplex–generalized severe type due to keratin 5 p.Glu477Lys mutation: Genotype‐phenotype correlation and in silico modeling analysis

Pediatric dermatology, 2019-01, Vol.36 (1), p.132-138

2019

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New insight into mechanisms of pruritus from molecular studies on familial primary localized cutaneous amyloidosis

British journal of dermatology (1951), 2009-12, Vol.161 (6), p.1217-1224

2009

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APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa

Science translational medicine, 2018-08, Vol.10 (455)

2018

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Replenishment of type VII collagen and re-epithelialization of chronically ulcerated skin after intradermal administration of allogeneic mesenchymal stromal cells in two patients with recessive dystrophic epidermolysis bullosa

Cytotherapy (Oxford, England), 2010, Vol.12 (3), p.429-431

2010

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LB1007 Analysis of chemokines in blister fluids of epidermolysis bullosa patients: Implications for therapy

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.B13-B13

2017

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Reduced Microbial Diversity Is a Feature of Recessive Dystrophic Epidermolysis Bullosa-Involved Skin and Wounds

Journal of investigative dermatology, 2018-11, Vol.138 (11), p.2492-2495

2018

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Balint's syndrome revealing Creutzfeldt-Jakob disease

Interprofessional recommendations on behalf of Société française de radiothérapie oncologique for the prevention, protection and management of cyberattacks in radiation oncology

Prévention, protection, et gestion des cyberattaques en oncologie radiothérapie : recommandations interprofessionnelles au nom de la Société française de radiothérapie oncologique

Radiothérapie externe du sein et des aires ganglionnaires : étude dosimétrique multicentrique

Dosimetric Evaluation of Modulated ArcTherapy (DEMAT)

22- A multi-center study of breast irradiation techniques

14 - Dosimetric Evaluation of Modulated ArcTherapy (DEMAT)

Clinical aspects and usefulness of indirect absorbed immunofluorescence for diagnosis of yaws in Central Africa

Anti-(human LFA-1) monoclonal antibodies bind P815 murine tumour cells

Analysis of the Gc polymorphism in human populations by isoelectrofocusing on polyacrylamide gels. Demonstration of subtypes of the Gc allele and of additional Gc variants

The health of Central African students at the time of their arrival in France

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines

Diagnosis and management of pemphigus: Recommendations of an international panel of experts

550 Daclatasvir improves life quality in murine recessive dystrophic epidermolysis bullosa

Analysis of the Gc polymorphism in human populations by isoelectrofocusing on polyacrylamide gels. Demonstration of subtypes of the Gc1 allele and of additional Gc variants

Patients suffering from dystrophic epidermolysis bullosa are prone to developing autoantibodies against skin proteins: A longitudinal confirmational study

Gc, Tf, Hp subtype and alpha 1-antitrypsin polymorphisms in a Pygmy Bi-Aka sample

Molecular epidemiology of junctional epidermolysis bullosa: discovery of novel and frequent LAMB3 mutations in Chilean patients with diagnostic significance

Epidermolysis bullosa simplex–generalized severe type due to keratin 5 p.Glu477Lys mutation: Genotype‐phenotype correlation and in silico modeling analysis

New insight into mechanisms of pruritus from molecular studies on familial primary localized cutaneous amyloidosis

APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa

Replenishment of type VII collagen and re-epithelialization of chronically ulcerated skin after intradermal administration of allogeneic mesenchymal stromal cells in two patients with recessive dystrophic epidermolysis bullosa

LB1007 Analysis of chemokines in blister fluids of epidermolysis bullosa patients: Implications for therapy

Reduced Microbial Diversity Is a Feature of Recessive Dystrophic Epidermolysis Bullosa-Involved Skin and Wounds

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