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7. Exploring the phenotypic spectrum and osteopenia mechanisms in Yunis-Varón syndrome

8. Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation

18. Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals

19. Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans

24. Evaluating ecotoxicological assays for comprehensive risk assessment of toxic metals present in industrial wastewaters in the Republic of Korea

25. Méthodes de recueil et report des données épidémiologiques sur les blessures et les maladies dans le sport : synthèse ReFORM de la position de consensus du Comité international olympique

26. Findings from the Morquio A Registry Study (MARS) after 6 years: Long-term outcomes of MPS IVA patients treated with elosulfase alfa

30. Development of a core outcome set for mucopolysaccharidoses (MPS) in children: Results from Delphi surveys and a consensus workshop

36. A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder

37. N-functionalized hierarchical carbon composite derived from ZIF-67 and carbon foam for efficient overall water splitting

41. PIGG variant pathogenicity assessment reveals characteristic features within 19 families

42. Findings from the Morquio A Registry Study (MARS) after 6 years: Long-term outcomes of MPS IVA patients treated with elosulfase alfa

47. Oxygen vacancy modification of commercial ZnO by hydrogen reduction for the removal of thiabendazole: Characterization and kinetic study

48. Surpassing the 1 Li/Ti capacity limit in chlorine modified TiO2−yCl2y

49. Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome

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