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36 results on '"Salles, Jean Pierre"'

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1. Plasma p-tau181 as an outcome and predictor of multidomain intervention effects: a secondary analysis of a randomised, controlled, dementia prevention trial

2. Diagnostic yield of bone fragility gene panel sequencing in children and young adults referred for idiopathic primary osteoporosis at a single regional reference centre

3. Prenatal features and neonatal management of severe hyperparathyroidism caused by the heterozygous inactivating calcium-sensing receptor variant, Arg185Gln: A case report and review of the literature

4. Low bone mass in Noonan syndrome children correlates with decreased muscle mass and low IGF-1 levels

7. SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome

8. Utility of genetic testing for prenatal presentations of hypophosphatasia

9. Ghrelin uses the GHS-R1a/Gi/cAMP pathway and induces differentiation only in mature osteoblasts. This ghrelin pathway is impaired in AIS patients

10. Glycerophosphodiesterase 3 (GDE3) is a lysophosphatidylinositol-specific ectophospholipase C acting as an endocannabinoid signaling switch

11. Meal-related difficulties and weight loss in older people: Longitudinal data from MAPT study

12. The type 1 lysophosphatidic acid receptor is involved in osteoblastogenesis up to osteocytogenesis

13. Expression of the type 1 lysophosphatidic acid receptor in osteoblastic cell lineage controls both bone mineralization and osteocyte specification

14. Red blood cell membrane omega-3 fatty acid levels and physical performance: Cross-sectional data from the MAPT study

16. Effect of long-term omega 3 polyunsaturated fatty acid supplementation with or without multidomain intervention on cognitive function in elderly adults with memory complaints (MAPT): a randomised, placebo-controlled trial

17. Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS

19. Molecular diagnosis of hypophosphatasia and differential diagnosis by targeted Next Generation Sequencing

22. Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass

30. Human epidermis is a novel site of phospholipase B expression

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