305 results on '"Tauber, Maithé"'
Search Results
52. New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity
53. Physical Activity in Patients with Prader-Willi Syndrome—A Systematic Review of Observational and Interventional Studies
54. SHP2 drives inflammation-triggered insulin resistance by reshaping tissue macrophage populations
55. Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network
56. Factors associated with overweight in preschool-age children in southwestern France
57. Truncal Distribution of Fat Mass, Metabolic Profile and Hypothalamic-Pituitary Adrenal Axis Activity in Prepubertal Obese Children
58. Effects of the COVID-19 pandemic and lockdown on the mental and physical health of adults with Prader-Willi Syndrome
59. Wrist anomalies in Turner syndrome compared with Leri-Weill dyschondrosteosis: a new feature in Turner syndrome
60. Puberté précoce
61. IMAGe association and congenital adrenal hypoplasia: No disease-causing mutations found in the ACD gene
62. Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human
63. Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity
64. What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders?
65. Effects of the COVID-19 pandemic and lockdown on the mental and physical health of adults with Prader-Willi Syndrome
66. Setmelanotide for controlling weight and hunger in Bardet-Biedl syndrome
67. Adolescents with Partial Growth Hormone (GH) Deficiency Develop Alterations of Body Composition after GH Discontinuation and Require Follow-Up
68. Acquired von Willebrand’s syndrome caused by primary hypothyroidism in a 5-year-old girl
69. Prader‐Willi syndrome: A model for understanding the ghrelin system
70. Noonan syndrome males display Sertoli cell-specific primary testicular insufficiency
71. Prenatal education of overweight or obese pregnant women to prevent childhood overweight (the ETOIG study): an open-label, randomized controlled trial
72. Noonan syndrome-causing SHP2 mutants impair ERK-dependent chondrocyte differentiation during endochondral bone growth
73. Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome
74. AZP-531, an unacylated ghrelin analog, improves food-related behavior in patients with Prader-Willi syndrome: A randomized placebo-controlled trial
75. Functional Effects of PTPN11 (SHP2) Mutations Causing LEOPARD Syndrome on Epidermal Growth Factor-Induced Phosphoinositide 3-Kinase/AKT/Glycogen Synthase Kinase 3β Signaling
76. A model to characterize psychopathological features in adults with Prader-Willi syndrome
77. Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome
78. Meta-Analysis of Paediatric Patients with Central Precocious Puberty Treated with Intramuscular Triptorelin 11.25 mg 3-Month Prolonged-Release Formulation
79. High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome.
80. Aspects biologiques, moléculaires et cliniques de l'axe GH/IGF-I
81. Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi Syndrome
82. Bridging the gap: metabolic and endocrine care of patients during transition
83. High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome
84. Growth patterns of patients with Noonan syndrome: correlation with age and genotype
85. Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi Syndrome: a matched control study
86. Chapitre 5 - Puberté précoce
87. Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation
88. Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age andFBN1Genotype
89. Haploinsufficiency of the miR-873/miR-876 microRNA cluster is associated with craniofacial abnormalities
90. Polyvalvular heart disease with joint hypermobility, characteristic facies, and particular skin abnormalities: New cases of “polyvalvular heart disease syndrome” or new association?
91. Clinical utility gene card for: Prader-Willi Syndrome
92. Les dépressions
93. Behavioral profile of adults with Prader-Willi syndrome : correlations with individual and environmental variables
94. Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human.
95. Comparison of response to 2-years' growth hormone treatment in children with isolated growth hormone deficiency, born small for gestational age, idiopathic short stature, or multiple pituitary hormone deficiency: combined results from two large observational studies.
96. Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS
97. A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk
98. Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables
99. Gonadotropin-Releasing Hormone Agonist Treatment in Sexual Precocity.
100. Comparison of response to 2-years’ growth hormone treatment in children with isolated growth hormone deficiency, born small for gestational age, idiopathic short stature, or multiple pituitary hormone deficiency: combined results from two large observational studies
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