Search

Your search keyword '"Robert, Matthieu"' showing total 407 results

Search Constraints

Start Over You searched for: Author "Robert, Matthieu" Remove constraint Author: "Robert, Matthieu"
407 results on '"Robert, Matthieu"'

Search Results

1. Ocular sequelae of epidermal necrolysis: French national audit of practices, literature review and proposed management

2. StorAlloc: A Simulator for Job Scheduling on Heterogeneous Storage Resources

3. Extraction of Nystagmus Patterns from Eye-Tracker Data with Convolutional Sparse Coding

4. Long term follow-up after haematopoietic stem cell transplantation for mucopolysaccharidosis type I-H: a retrospective study of 51 patients

6. Congenital aniridia beyond black eyes: From phenotype and novel genetic mechanisms to innovative therapeutic approaches

10. The role of irinotecan-bevacizumab as rescue regimen in children with low-grade gliomas: a retrospective nationwide study in 72 patients

12. Auteurs et collaborateurs

15. PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review

16. Ocular Motor Apraxia

19. GPATCH11 variants cause mis-splicing and early-onset retinal dystrophy with neurological impairment

20. Ceroid lipofuscinosis type 2 disease: Effective presymptomatic therapy—Oldest case of a presymptomatic enzyme therapy.

21. Sostdc1 is expressed in all major compartments of developing and adult mammalian eyes

22. Weill-Marchesani syndrome: natural history and genotype-phenotype correlations from 18 news cases and review of literature.

24. GPATCH11variants cause mis-splicing and early-onset retinal dystrophy with neurological impairment

29. Acute tubulointerstitial nephritis with or without uveitis: a novel form of post-acute COVID-19 syndrome in children

34. Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy

37. Les auteurs

38. Long term follow-up after haematopoietic stem cell transplantation for mucopolysaccharidosis type I-H: a retrospective study of 51 patients

43. Oculo-Cutaneous Albinism Type 4 (OCA4): Phenotype-Genotype Correlation

44. Congenital aniridia beyond black eyes: From phenotype and novel genetic mechanisms to innovative therapeutic approaches

45. Supporting Dynamic Allocation of Heterogeneous Storage Resources on HPC Systems

46. Myopia: Insights from a population‐based survey.

47. Reply

48. Neuroinflammatory Disease following Severe Acute Respiratory Syndrome Coronavirus 2 Infection in Children

Catalog

Books, media, physical & digital resources