Pesquisa | Portal de Pesquisa da BVS Enfermagem

1.

Critical body fat percentage required for puberty onset: the Taiwan Pubertal Longitudinal Study.

Huang, L; Hou, J-W; Fan, H-Y; Tsai, M-C; Yang, C; Hsu, J B; Chen, Y C.

J Endocrinol Invest ; 46(6): 1177-1185, 2023 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-36436189

2.

Sources of cholesterol for testosterone biosynthesis in murine Leydig cells.

Hou, J W; Collins, D C; Schleicher, R L.

Endocrinology ; 127(5): 2047-55, 1990 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-2226298

3.

Kleine-Levin syndrome in a boy with Prader-Willi syndrome.

Gau, S F; Soong, W T; Liu, H M; Hou, J W; Tsai, W Y; Chiu, Y N; Yeh, Y C; Wang, P J; Wang, T R.

Sleep ; 19(1): 13-7, 1996 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-8650457

4.

Galloway-Mowat syndrome in Taiwan.

Hou, J W; Wang, T R.

Am J Med Genet ; 58(3): 245-8, 1995 Sep 11.

Artigo em Inglês | MEDLINE | ID: mdl-8533826

5.

Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect.

Hsieh, Y C; Hou, J W.

Am J Med Genet ; 86(3): 278-81, 1999 Sep 17.

Artigo em Inglês | MEDLINE | ID: mdl-10482880

6.

Jacobsen distal 11q deletion syndrome with a myelodysplastic change of hemopoietic cells.

Lin, J H; Hou, J W; Teng, R J; Tien, H F; Lin, K H.

Am J Med Genet ; 75(4): 341-4, 1998 Feb 03.

Artigo em Inglês | MEDLINE | ID: mdl-9482638

7.

Prognostic significance of left ventricular diastolic indexes in beta-thalassemia major.

Hou, J W; Wu, M H; Lin, K H; Lue, H C.

Arch Pediatr Adolesc Med ; 148(8): 862-6, 1994 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-8044266

8.

Optimization of walking in children.

Jeng, S F; Liao, H F; Lai, J S; Hou, J W.

Med Sci Sports Exerc ; 29(3): 370-6, 1997 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-9139176

9.

Growth of bifidobacteria in soymilk and their survival in the fermented soymilk drink during storage.

Chou, C C; Hou, J W.

Int J Food Microbiol ; 56(2-3): 113-21, 2000 Jun 01.

Artigo em Inglês | MEDLINE | ID: mdl-10857537

10.

Angelman syndrome assessed by neurological and molecular cytogenetic investigations.

Hou, J W; Wang, P J; Wang, T R.

Pediatr Neurol ; 16(1): 17-22, 1997 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-9044396

11.

Homocystinuria presenting as fatal common carotid artery occlusion.

Lu, C Y; Hou, J W; Wang, P J; Chiu, H H; Wang, T R.

Pediatr Neurol ; 15(2): 159-62, 1996 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-8888052

12.

MR imaging in patients with strabismus.

Hou, J W; Fukatsu, H; Ishigaki, T.

Chin Med J (Engl) ; 107(8): 631-5, 1994 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-7805451

13.

ESR spin trapping studies on the free radicals in gasphase of cigarette smoking.

Zhao, B L; Yan, L J; Hou, J W; Xin, W J.

Chin Med J (Engl) ; 104(7): 591-4, 1991 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-1652410

14.

Active oxygen radicals produced by leukocytes of malignant lymphoma.

Li, X J; Zhao, B L; Hou, J W; Xin, W J; Xie, R F; Chen, Y R.

Chin Med J (Engl) ; 103(11): 899-905, 1990 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-2177391

15.

Cytogenetic investigations in trisomy 21 with reciprocal 4/9 translocation: report of a case.

Hou, J W; Wang, T R.

J Formos Med Assoc ; 93(11-12): 958-60, 1994.

Artigo em Inglês | MEDLINE | ID: mdl-7633202

16.

Idiopathic juvenile osteoporosis: five-year case follow-up.

Hou, J W; Wang, T R.

J Formos Med Assoc ; 94(5): 277-80, 1995 May.

Artigo em Inglês | MEDLINE | ID: mdl-7613264

17.

Primed in situ (PRINS) labeling for rapid detection of numeric and structural chromosome anomalies.

Hou, J W; Wang, T R.

J Formos Med Assoc ; 96(1): 46-50, 1997 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-9033182

18.

Prader-Willi syndrome: clinical and molecular cytogenetic investigations.

Hou, J W; Wang, T R.

J Formos Med Assoc ; 95(6): 474-9, 1996 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-8772055

19.

Double aneuploidy with Down's-Klinefelter's syndrome.

Hou, J W; Wang, T R.

J Formos Med Assoc ; 95(4): 350-2, 1996 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-8935309

20.

Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiency.

Hou, J W; Wang, T R.

J Formos Med Assoc ; 95(2): 144-7, 1996 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-9064003

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Critical body fat percentage required for puberty onset: the Taiwan Pubertal Longitudinal Study.

Sources of cholesterol for testosterone biosynthesis in murine Leydig cells.

Kleine-Levin syndrome in a boy with Prader-Willi syndrome.

Galloway-Mowat syndrome in Taiwan.

Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect.

Jacobsen distal 11q deletion syndrome with a myelodysplastic change of hemopoietic cells.

Prognostic significance of left ventricular diastolic indexes in beta-thalassemia major.

Optimization of walking in children.

Growth of bifidobacteria in soymilk and their survival in the fermented soymilk drink during storage.

Angelman syndrome assessed by neurological and molecular cytogenetic investigations.

Homocystinuria presenting as fatal common carotid artery occlusion.

MR imaging in patients with strabismus.

ESR spin trapping studies on the free radicals in gasphase of cigarette smoking.

Active oxygen radicals produced by leukocytes of malignant lymphoma.

Cytogenetic investigations in trisomy 21 with reciprocal 4/9 translocation: report of a case.

Idiopathic juvenile osteoporosis: five-year case follow-up.

Primed in situ (PRINS) labeling for rapid detection of numeric and structural chromosome anomalies.

Prader-Willi syndrome: clinical and molecular cytogenetic investigations.

Double aneuploidy with Down's-Klinefelter's syndrome.

Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiency.