Mignot Cyril | Ap-hp Reference Center For Lysosomal Diseases Neuropediatric Unit Hopital Armand Trousseau
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概要
- MIGNOT Cyrilの詳細を見る
- 同名の論文著者
- Ap-hp Reference Center For Lysosomal Diseases Neuropediatric Unit Hopital Armand Trousseauの論文著者
関連著者
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Mignot Cyril
Ap-hp Service De Neuropediatrie Hopital Armand Trousseau
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Mignot Cyril
Ap-hp Reference Center For Lysosomal Diseases Neuropediatric Unit Hopital Armand Trousseau
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MIGNOT Cyril
AP-HP, Service de Neuropediatrie, Hopital Armand Trousseau
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DESGUERRE Isabelle
AP-HP, Service de Neuropediarie, Hopital Necker-Enfants Malades
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BURGLEN Lydie
AP-HP, Service de Genetique, Hopital Armand Trousseau
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HERTZ-PANNIER Lucie
AP-HP, Service de Radiologie Pediatrique, Hopital Necker-Enfants Malades
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RENALDO Florence
AP-HP, Service de Neuropediatrie, Hopital Armand Trousseau
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GADISSEUX Jean-Francois
Hopital Prive d' Antony
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GALLET Serge
Serge Gallet, Service de Pediatrie, Centre hospitalier de Montlucon
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PHAM-DINH Danielle
AP-HP, Service de Neuropediatrie, Hopital Armand Trousseau
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BOESPFLUG-TANGUY Odile
Service de Genetique Medicale, CHU de Clermont-Ferrand, Hotel Dieu
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RODRIGUEZ Diana
AP-HP, Service de Neuropediatrie, Hopital Armand Trousseau
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Gallet Serge
Serge Gallet Service De Pediatrie Centre Hospitalier De Montlucon
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Burglen Lydie
Ap-hp Service De Genetique Hopital Armand Trousseau
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Renaldo Florence
Ap-hp Service De Neuropediatrie Hopital Armand Trousseau
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Desguerre Isabelle
Ap-hp Service De Neuropediarie Hopital Necker-enfants Malades
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Pham-dinh Danielle
Ap-hp Service De Neuropediatrie Hopital Armand Trousseau
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Hertz-pannier Lucie
Ap-hp Service De Radiologie Pediatrique Hopital Necker-enfants Malades
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Boespflug-tanguy Odile
Service De Genetique Medicale Chu De Clermont-ferrand Hotel Dieu
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Gadisseux Jean-francois
Hopital Prive D' Antony
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Rodriguez Diana
Ap-hp Service De Neuropediatrie Hopital Armand Trousseau
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De Villemeur
Institut Cochin Universite Paris Descartes Cnrs (umr 8104) Inserm
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KRAOUA Ichraf
AP-HP, Reference Center for Lysosomal Diseases, Nervous System Disease Federation, Hopital de la Sal
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SEDEL Frederic
AP-HP, Reference Center for Lysosomal Diseases, Nervous System Disease Federation, Hopital de la Sal
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CAILLAUD Catherine
Institut Cochin, Universite Paris Descartes, CNRS (UMR 8104), INSERM
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FROISSART Roseline
Laboratory of Hereditary Metabolic Disorders, Centre de Biologie et de Pathologie Est, Hospices Civi
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STIRNEMANN Jerome
AP-HP, Reference Center for Lysosomal Diseases, Department of Internal Medicine, Hopital Jean Verdie
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CHAURAND Guy
Department of Pediatrics, Hopital Saint-Pierre
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FLODROPS Hugues
Department of Pediatrics, Hopital Saint-Pierre
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TARI Saliha
Department of Pediatrics, CHU Beni Messous
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GOURFINKEL-AN Isabelle
AP-HP, Epileptology Unit, Centre de Reference des Epilepsies Rares, Hopital de la Salpetriere
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MATHIEU Sophie
AP-HP, Reference Center for Lysosomal Diseases, Neuropediatric Unit, Hopital Armand Trousseau
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BELMATOUG Nadia
AP-HP, Reference Center for Lysosomal Diseases, Department of Internal Medicine, Hopital Beaujon
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Tari Saliha
Department Of Pediatrics Chu Beni Messous
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Chaurand Guy
Department Of Pediatrics Hopital Saint-pierre
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Kraoua Ichraf
Ap-hp Reference Center For Lysosomal Diseases Nervous System Disease Federation Hopital De La Salpet
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Mathieu Sophie
Ap-hp Reference Center For Lysosomal Diseases Neuropediatric Unit Hopital Armand Trousseau
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Sedel Frederic
Ap-hp Reference Center For Lysosomal Diseases Nervous System Disease Federation Hopital De La Salpet
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Belmatoug Nadia
Ap-hp Reference Center For Lysosomal Diseases Department Of Internal Medicine Hopital Beaujon
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Flodrops Hugues
Department Of Pediatrics Hopital Saint-pierre
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Stirnemann Jerome
Ap-hp Reference Center For Lysosomal Diseases Department Of Internal Medicine Hopital Jean Verdier
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Froissart Roseline
Laboratory Of Hereditary Metabolic Disorders Centre De Biologie Et De Pathologie Est Hospices Civils
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Gourfinkel-an Isabelle
Ap-hp Epileptology Unit Centre De Reference Des Epilepsies Rares Hopital De La Salpetriere
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Caillaud Catherine
Institut Cochin Universite Paris Descartes Cnrs (umr 8104) Inserm
著作論文
- Tumor-like enlargement of the optic chiasm in an infant with Alexander disease
- A French experience of type 3 Gaucher disease : Phenotypic diversity and neurological outcome of 10 patients