Detalles de la búsqueda
1.
Factors associated with low bone mineral density in Turner syndrome: a multicenter prospective observational study.
Endocr J;
2024 Mar 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-38522940
2.
Detection of multiple druggable mutations of lung cancer from cytology specimens by MINtS: An advanced medicine A trial.
Cancer Sci;
114(8): 3342-3351, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37139543
3.
Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty.
Endocr J;
70(1): 59-67, 2023 Jan 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-36216557
4.
Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation.
Cytogenet Genome Res;
162(11-12): 617-624, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-37231804
5.
Identification of clinical factors related to antibody-mediated immune response to the subfornical organ.
Clin Endocrinol (Oxf);
97(1): 72-80, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35419873
6.
Current status of transition medicine for 21-hydroxylase deficiency in Japan: from the perspective of pediatric endocrinologists.
Endocr J;
69(1): 75-83, 2022 Jan 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-34373418
7.
Starting age of oestrogen-progestin therapy is negatively associated with bone mineral density in young adults with Turner syndrome independent of age and body mass index.
Clin Endocrinol (Oxf);
95(1): 84-91, 2021 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-33872421
8.
Rapid Hypercalciuria Induction With Bone Formation Marker Reduction During Immobilization in Children.
Endocr Pract;
27(10): 998-1003, 2021 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-34098084
9.
SOX9 is colocalized with paraspeckle protein NONO in cultured murine sertoli cells and features structural characteristics of intrinsically disordered proteins.
Mol Reprod Dev;
87(11): 1124-1125, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-33022123
10.
A retrospective multicenter study of bone mineral density in adolescents and adults with Turner syndrome in Japan.
Endocr J;
67(10): 1023-1028, 2020 Oct 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-32554947
11.
Language delay and developmental catch-up would be a clinical feature of pseudohypoparathyroidism type 1A during childhood.
Endocr J;
66(3): 215-221, 2019 Mar 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-30674755
12.
Diagnosis of congenital hyperinsulinism: Biochemical profiles during hypoglycemia.
Pediatr Diabetes;
19(2): 259-264, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-28597971
13.
Integrated treatment for autonomic paraneoplastic syndrome improves performance status in a patient with small lung cell carcinoma: a case report.
BMC Neurol;
18(1): 189, 2018 Nov 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30414621
14.
Incidence rate and characteristics of symptomatic vitamin D deficiency in children: a nationwide survey in Japan.
Endocr J;
65(6): 593-599, 2018 Jun 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-29526992
15.
Graves' disease as an emerging complication of MIRAGE syndrome.
Pediatr Int;
65(1): e15678, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37888342
16.
FGFR1 Analyses in Four Patients with Hypogonadotropic Hypogonadism with Split-Hand/Foot Malformation: Implications for the Promoter Region.
Hum Mutat;
38(5): 503-506, 2017 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28087897
17.
Use of liothyronine without levothyroxine in the treatment of mild consumptive hypothyroidism caused by hepatic hemangiomas.
Endocr J;
64(6): 639-643, 2017 Jun 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-28420821
18.
Hypertension is a characteristic complication of X-linked hypophosphatemia.
Endocr J;
64(3): 283-289, 2017 Mar 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-28025445
19.
Free T3 to free T4 ratio less than 2.0 suggests low T3 syndrome rather than central hypothyroidism from the age of two to eighteen years.
Endocr J;
64(2): 213-219, 2017 Feb 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-28003587
20.
Homozygous DUOXA2 mutation (p.Tyr138*) in a girl with congenital hypothyroidism and her apparently unaffected brother: Case report and review of the literature.
Endocr J;
64(8): 807-812, 2017 Aug 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-28626131