Detalhe da pesquisa
1.
Identification of novel compound heterozygous variants in the SLC30A7 (ZNT7) gene in two French brothers with stunted growth, testicular hypoplasia and bone marrow failure.
Hum Mol Genet
; 32(12): 2016-2031, 2023 06 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36821639
2.
Outcomes of hybrid closed-loop insulin delivery activated 24/7 versus evening and night in free-living prepubertal children with type 1 diabetes: A multicentre, randomized clinical trial.
Diabetes Obes Metab
; 24(3): 511-521, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34816597
3.
Time trend in excess mortality in children with type 1 diabetes from 1987 to 2016 in mainland France.
Pediatr Diabetes
; 23(1): 38-44, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34881493
4.
Gene expression signatures predict response to therapy with growth hormone.
Pharmacogenomics J
; 21(5): 594-607, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34045667
5.
Increasing knowledge in IGF1R defects: lessons from 35 new patients.
J Med Genet
; 57(3): 160-168, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31586944
6.
GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty.
Hum Reprod
; 35(10): 2312-2322, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32862222
7.
Effects of advanced carbohydrate counting on glucose control and quality of life in children with type 1 diabetes.
Pediatr Diabetes
; 21(7): 1240-1248, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32644264
8.
Association of diabetic ketoacidosis and HbA1c at onset with year-three HbA1c in children and adolescents with type 1 diabetes: Data from the International SWEET Registry.
Pediatr Diabetes
; 21(2): 339-348, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31797499
9.
Forum theater staging of difficult encounters with patients to increase empathy in students: evaluation of efficacy at The University of Angers Medical School.
BMC Med Educ
; 20(1): 58, 2020 Feb 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-32093709
10.
Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations.
Hum Mutat
; 40(11): 2033-2043, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31231873
11.
Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disability.
Clin Genet
; 96(4): 354-358, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31290144
12.
Closed-loop driven by control-to-range algorithm outperforms threshold-low-glucose-suspend insulin delivery on glucose control albeit not on nocturnal hypoglycaemia in prepubertal patients with type 1 diabetes in a supervised hotel setting.
Diabetes Obes Metab
; 21(1): 183-187, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30047223
13.
Is there an optimal strategy for real-time continuous glucose monitoring in pediatrics? A 12-month French multi-center, prospective, controlled randomized trial (Start-In!).
Pediatr Diabetes
; 20(3): 304-313, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30663187
14.
Executive Functions in Children and Adolescents with Turner Syndrome: A Systematic Review and Meta-Analysis.
Neuropsychol Rev
; 28(2): 188-215, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29704077
15.
[Epidemiology of type 1 diabetes and its complications]. / Épidémiologie du diabète de type 1 et de ses complications.
Rev Prat
; 68(6): 607-610, 2018 Jun.
Artigo
em Francês
| MEDLINE | ID: mdl-30869246
16.
Congenital hypothyroidism and hearing loss without inner ear malformation: Think TPO.
Clin Genet
; 99(4): 604-606, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33368191
17.
Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control study.
BMC Public Health
; 16(1): 1021, 2016 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-27682602
18.
Association between altered placental human chorionic gonadotrophin (hCG) production and the occurrence of cryptorchidism: a retrospective study.
BMC Pediatr
; 14: 191, 2014 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25064170
19.
Heterozygous gain of function variant in GUCY1A2 may cause autonomous ovarian hyperfunction.
Eur J Endocrinol
; 190(4): 266-274, 2024 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38578777
20.
Insufficient Bone Mineralization to Sustain Mechanical Load of Weight in Obese Boys: A Cross-Sectional Study.
J Clin Endocrinol Metab
; 109(6): 1443-1453, 2024 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38163968