Serveur d'exploration sur les relations entre la France et l'Australie - Analysis (UK)

Index « Auteurs » - entrée « Inmaculada Calvo Penades »
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Inmaculada Andreu < Inmaculada Calvo Penades < Inmaculada Calvo Penadés  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 1.
Ident.Authors (with country if any)Title
000815 (2016) Nienke M. Ter Haar [Pays-Bas] ; Jerold Jeyaratnam [Pays-Bas] ; Helen J. Lachmann [Royaume-Uni] ; Anna Simon [Pays-Bas] ; Paul A. Brogan [Royaume-Uni] ; Matteo Doglio [Italie] ; Marco Cattalini [Italie] ; Jordi Anton [Espagne] ; Consuelo Modesto [Espagne] ; Pierre Quartier [France] ; Esther Hoppenreijs [Pays-Bas] ; Silvana Martino [Italie] ; Antonella Insalaco [Italie] ; Luca Cantarini [Italie] ; Loredana Lepore [Italie] ; Maria Alessio [Italie] ; Inmaculada Calvo Penades [Espagne] ; Christina Boros [Australie] ; Rita Consolini [Italie] ; Donato Rigante [Italie] ; Ricardo Russo [Argentine] ; Jana Pachlopnik Schmid [Suisse] ; Thirusha Lane [Royaume-Uni] ; Alberto Martini [Italie] ; Nicolino Ruperto [Italie] ; Joost Frenkel [Pays-Bas] ; Marco Gattorno [Italie]The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry.

List of associated KwdEn.i

Nombre de
documents
Descripteur
1Abdominal Pain (etiology)
1Abdominal Pain (genetics)
1Abdominal Pain (physiopathology)
1Adolescent
1Age of Onset
1Amyloidosis (etiology)
1Amyloidosis (genetics)
1Amyloidosis (physiopathology)
1Arthralgia (etiology)
1Arthralgia (genetics)
1Arthralgia (physiopathology)
1Arthritis (etiology)
1Arthritis (genetics)
1Arthritis (physiopathology)
1Cerebellar Diseases (etiology)
1Cerebellar Diseases (genetics)
1Cerebellar Diseases (physiopathology)
1Child
1Child, Preschool
1Conjunctivitis (etiology)
1Conjunctivitis (genetics)
1Conjunctivitis (physiopathology)
1Diarrhea (etiology)
1Diarrhea (genetics)
1Diarrhea (physiopathology)
1Female
1Genotype
1Headache (etiology)
1Headache (genetics)
1Headache (physiopathology)
1Humans
1Infant
1Infant, Newborn
1Intellectual Disability (etiology)
1Intellectual Disability (genetics)
1Intellectual Disability (physiopathology)
1Lymphadenopathy (etiology)
1Lymphadenopathy (genetics)
1Lymphadenopathy (physiopathology)
1Male
1Mevalonate Kinase Deficiency (complications)
1Mevalonate Kinase Deficiency (genetics)
1Mevalonate Kinase Deficiency (physiopathology)
1Myalgia (etiology)
1Myalgia (genetics)
1Myalgia (physiopathology)
1Pharyngitis (etiology)
1Pharyngitis (genetics)
1Pharyngitis (physiopathology)
1Phenotype
1Phosphotransferases (Alcohol Group Acceptor) (genetics)
1Registries
1Retrospective Studies
1Skin Diseases (etiology)
1Skin Diseases (genetics)
1Skin Diseases (physiopathology)
1Stomatitis, Aphthous (etiology)
1Stomatitis, Aphthous (genetics)
1Stomatitis, Aphthous (physiopathology)
1Uveitis (etiology)
1Uveitis (genetics)
1Uveitis (physiopathology)
1Vomiting (etiology)
1Vomiting (genetics)
1Vomiting (physiopathology)

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