Detalhe da pesquisa
1.
RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function.
Diabetologia
; 2024 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38743124
2.
Prenatal, newborn and childhood factors and the timing of puberty in boys and girls.
Pediatr Res
; 2024 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38594422
3.
During an 18-month course of automated insulin delivery treatment, children aged 2 to 6 years achieve and maintain a higher time in tight range.
Diabetes Obes Metab
; 26(6): 2431-2438, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38514384
4.
Health-related quality of life and self-reported health status in adolescents with chronic health conditions before transfer of care to adult health care: an international cohort study.
BMC Pediatr
; 24(1): 163, 2024 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38459510
5.
Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register.
Diabetologia
; 66(3): 438-449, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36418577
6.
A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY.
Diabetologia
; 65(4): 632-643, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34951657
7.
Onset and progression of puberty in Klinefelter syndrome.
Clin Endocrinol (Oxf)
; 96(3): 363-370, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34523156
8.
Serum testosterone and oestradiol predict the growth response during puberty promoting treatment.
Clin Endocrinol (Oxf)
; 96(2): 220-226, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34596269
9.
Cytosolic phosphoenolpyruvate carboxykinase deficiency: Expanding the clinical phenotype and novel laboratory findings.
J Inherit Metab Dis
; 45(2): 223-234, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34622459
10.
The effect of COVID-19 lockdown on the glycemic control of children with type 1 diabetes.
BMC Pediatr
; 22(1): 48, 2022 01 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35045807
11.
Bone structure assessed with pQCT in prepubertal males with delayed puberty or congenital hypogonadotropic hypogonadism.
Clin Endocrinol (Oxf)
; 95(1): 107-116, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33738832
12.
Familial central precocious puberty: two novel MKRN3 mutations.
Pediatr Res
; 90(2): 431-435, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33214675
13.
First year on commercial hybrid closed-loop system-experience on 111 children and adolescents with type 1 diabetes.
Pediatr Diabetes
; 22(6): 909-915, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34015178
14.
Treatment of gonadotropin deficiency during the first year of life: long-term observation and outcome in five boys.
Hum Reprod
; 34(5): 863-871, 2019 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31067328
15.
Correction to: A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY.
Diabetologia
; 65(5): 912, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35238956
16.
Congenital hypogonadotropic hypogonadism, functional hypogonadotropism or constitutional delay of growth and puberty? An analysis of a large patient series from a single tertiary center.
Hum Reprod
; 32(1): 147-153, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27927844
17.
Childhood growth in boys with congenital hypogonadotropic hypogonadism.
Pediatr Res
; 79(5): 705-9, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26720605
18.
In vivo activation of the PI3K-Akt pathway in mouse beta cells by the EGFR mutation L858R protects against diabetes.
Diabetologia
; 57(5): 970-9, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24493201
19.
Central precocious puberty in boys: secular trend and clinical features.
Eur J Endocrinol
; 190(3): 211-219, 2024 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38523472
20.
Pancreatic imaging in MEN1-comparison of conventional and somatostatin receptor positron emission tomography/computed tomography imaging in real-life setting.
Eur J Endocrinol
; 188(5): 421-429, 2023 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36943311