832 results on '"Maroteaux, P."'
Search Results
2. Synthesis of Ag3Sn Submicrometer Particles via an Adapted Polyol Process in View of Their Use As Die-Attach Material in Power Modules
3. Morphine withdrawal recruits lateral habenula cytokine signaling to reduce synaptic excitation and sociability
4. Translational studies support a role for serotonin 2B receptor (HTR2B) gene in aggression-related cannabis response
5. Positive regulation of raphe serotonin neurons by serotonin 2B receptors
6. Adiporon, an adiponectin receptor agonist acts as an antidepressant and metabolic regulator in a mouse model of depression
7. Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research
8. Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis
9. Within-strain variation in behavior differs consistently between common inbred strains of mice
10. Regulation of raphe serotonin neurons by serotonin 1A and 2B receptors
11. Anomalien des Typ-II-Kollagens in Chondrodysplasien
12. 5-HT2B receptors are required for serotonin-selective antidepressant actions
13. Functions of serotonin in hypoxic pulmonary vascular remodeling
14. Metaphyseal anadysplasia type II: a new regressive metaphyseal dysplasia
15. Presentation of six cases of Stüve-Wiedemann syndrome
16. An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses
17. Revisiting metatropic dysplasia: Presentation of a series of 19 novel patients and review of the literature
18. Genetic mapping of Xp22.12–p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL)
19. Mutations in three subdomains of the carboxy-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasias
20. Acral dysostosis dyserythropoiesis syndrome
21. Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene
22. A dominant mutation in the COL1A1 gene that substitutes glycine for valine causes recurrent lethal osteogenesis imperfecta
23. International classification of osteochondrodysplasias
24. Cartilage hair hypoplasia in infancy: A misleading chondrodysplasia
25. Desbuquois syndrome
26. Dominant mutations in familial lethal and severe osteogenesis imperfecta
27. The spondylometaphyseal dysplasias. A tentative classification
28. Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3
29. Clinical, radiological, and chondro-osseous findings in opsismodysplasia: survey of a series of 12 unreported cases
30. An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature
31. Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance
32. Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?
33. Dyssegmental dysplasia: a case report of a Rolland-Desbuquois type
34. Desbuquois syndrome presenting with severe neonatal dwarfism, spondylo-epiphyseal dysplasia and advanced carpal bone age
35. A new type of chondrodysplasia punctata associated with peroxisomal dysfunction
36. Spondyloepiphyseal dysplasia of Maroteaux.
37. ÉTUDE GÉNÉTIQUE DU GARGOYLISME
38. GÉNÉTIQUE DE L'HÉMOCHROMATOSE
39. International Union of Basic and Clinical Pharmacology. CX. Classification of Receptors for 5-hydroxytryptamine; Pharmacology and Function
40. Desbuquois syndrome: clinical, radiographic and long-term outcome in 15 cases
41. Achondroplasia — A Clinician’s Viewpoint
42. Acromicric dysplasia: long-term outcome and evidence of autosomal dominant inheritance
43. Acromesomelic Dwarfism
44. Recessive lethal chondrodysplasia, “round femoral inferior epiphysis type”
45. Dinoflagellates in evolution. A molecular phylogenetic analysis of large subunit ribosomal RNA
46. Hypochondrogenesis
47. Leri's melorheostosis: Three pediatric cases and a review of the literature
48. A variant of mucolipidosis: II. Clinical, biochemical and pathological investigations
49. Achondrogenesis within the scope of connately manifested generalized skeletal dysplasias
50. The mild form of pseudoachondroplasia: Identity of the morphological and biochemical alterations of growth cartilage with those of typical pseudoachondroplasia
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.