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679 results on '"Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Robert Debré"'

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1. Impact of hydroxychloroquine used as DMARD on SARS-CoV-2 tests and infection evolution in a population of 871 patients with inflammatory rheumatic and musculoskeletal diseases

2. Effet d’un traitement par hydroxychloroquine prescrit comme traitement de fond de rhumatismes inflammatoires chroniques ou maladies auto-immunes systémiques sur les tests diagnostiques et l’évolution de l’infection à SARS CoV-2 : étude de 871 patients☆

3. Cost-effectiveness threshold of first-trimester Down syndrome maternal serum screening for the use of cell-free DNA as a second-tier screening test

4. X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

5. Simple and accurate quantitative analysis of cefiderocol and ceftobiprole in human plasma using liquid chromatography-isotope dilution tandem mass spectrometry: interest for their therapeutic drug monitoring and pharmacokinetic studies

6. Initiating antiretroviral treatment early in infancy has long-term benefits on the HIV reservoir in late childhood and adolescence

7. Hypertension in Children and Adolescents: A Position Statement From a Panel of Multidisciplinary Experts Coordinated by the French Society of Hypertension

8. [Acute abdominal and lumbar pain in children and adult]

9. Catatonia in a patient with Aicardi-Goutières syndrome efficiently treated with immunoadsorption

10. A toxic palmitoylation of Cdc42 enhances NF-κB signaling and drives a severe autoinflammatory syndrome

11. Risks of severe hyponatremia in children receiving hypotonic fluids

12. Vestibular Functioning in Children with Neurodevelopmental Disorders Using the Functional Head Impulse Test

13. Vaccine-preventable meningitis in French children with incorrect vaccination status from 2011 to 2013

14. Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura

15. Myelination induction by a histamine H3 receptor antagonist in a mouse model of preterm white matter injury

16. Impact of mutations within the [Fe-S] cluster or the lipoic acid biosynthesis pathways on mitochondrial protein expression profiles in fibroblasts from patients

17. Congenital Hypothyroidism: Role of Nuclear Medicine

18. CD117hi expression identifies a human fetal Hematopoietic Stem Cell population with high proliferation and self-renewal potential

19. Deleterious mutations in ALDH1L2 suggest a novel cause for neuro-ichthyotic syndrome

20. Homozygous GRN mutations: unexpected phenotypes and new insights into pathological and molecular mechanisms: New insights in homozygous GRN mutations

21. The Effect of Dual Task on Attentional Performance in Children With ADHD

22. Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France

23. A new AMPK activator, GSK773, corrects fatty acid oxidation and differentiation defect in CPT2-deficient myotubes

24. SLC13A3 variants cause acute reversible leukoencephalopathy and α-ketoglutarate accumulation

25. Oxytocin receptor agonist reduces perinatal brain damage by targeting microglia

26. Supplementary data to: Algorithms to define abnormal growth in children: external validation and head-to-head 3 comparison 4 5

27. Should 45,X/46,XY boys with no or mild anomaly of external genitalia be investigated and followed up?

28. Incidence of infantile Pompe disease in the Maroon population of French Guiana

29. Complex Association of Sex Hormones on Left Ventricular Systolic Function: Insight into Sexual Dimorphism

30. PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects

31. Functional ultrasound imaging of brain activity in human newborns

32. Autosomal recessive primary microcephaly due to ASPM mutations: An update

33. Paradoxical inhibition of glycolysis by pioglitazone opposes the mitochondriopathy caused by AIF deficiency

34. A framework to identify contributing genes in patients with Phelan-McDermid syndrome

35. Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

36. Novel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability

37. Mice with a deletion of the major central myelin protein exhibit hypersensitivity to noxious thermal stimuli: involvement of central sensitization

38. Pro-epileptogenic effects of viral-like inflammation in both mature and immature brains

39. Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation

40. Phenotypic effects of genetic variants associated with autism

41. Bench to Cribside: the Path for Developing a Neuroprotectant

42. QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver disease

43. ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects

44. Spontaneous fertility and pregnancy outcomes amongst 480 women with Turner syndrome

45. Patient/family views on data sharing in rare diseases: study in the European LeukoTreat project.: Survey assessing data sharing in leukodystrophies

46. Patient/family views on data sharing in rare diseases: study in the European LeukoTreat project.: Survey assessing data sharing in leukodystrophies

47. Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory

48. Mutation update for Kabuki syndrome genes KMT2D and KDM6A and further delineation of X-linked Kabuki syndrome subtype 2

49. A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome

50. Patient/family views on data sharing in rare diseases: study in the European LeukoTreat project.: Survey assessing data sharing in leukodystrophies

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