Co-authors (79)

Journals (13)

Keywords (34)

Embed

Academic

Authors

Noritaka Iwatani

Noritaka Iwatani,Kumamoto University,Endocrinology,Genetics & Genealogy,Family Medicine

Edit

Noritaka Iwatani

Kumamoto University

Publications: 16 | Citations: 147

Fields: Endocrinology, Genetics & Genealogy, Family Medicine

Collaborated with 79 co-authors from 1987 to 2004 | Cited by 688 authors

Cumulative Annual

Sort by:

Publications (16)

BibTeX | RIS | RefWorks Download

Learning and memorization impairment in childhood chronic fatigue syndrome manifesting as school phobia in Japan (Citations: 19)

, , , ,

Journal: Brain & Development - BRAIN DEVELOP , vol. 26, no. 7, pp. 442-447, 2004

Effects of exogenous melatonin on pituitary hormones in humans (Citations: 6)

, , ,

Journal: Clinical Physiology - CLIN PHYSIOL , vol. 21, no. 3, pp. 292-299, 2001

Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure (Citations: 51)

, , , ,

Journal: Journal of Pediatrics - J PEDIAT , vol. 137, no. 2, pp. 272-276, 2000

Prevalence of GH1 Gene Deletion in Patients with Isolated Growth Hormone Deficiency in Japan (Citations: 2)

, , , , , , ,

Journal: Endocrine Journal - ENDOCR J , vol. 47, no. 2, pp. 157-162, 2000

High-dose growth hormone (GH) treatment in prepubertal GH-deficient children (Citations: 5)

, , , , , , , , , , , http://academic.research.microsoft.com/io.ashx?type=5&id=33910703&selfId1=21504260&selfId2=0&maxNumber=12&query=

Journal: Acta Paediatrica - ACTA PAEDIAT , vol. 88, no. s428, pp. 76-79, 1999

Sort by:

Citations (147 times by 143 publications)

Brain-Lung-Thyroid Disease: Clinical Features of a Kindred With a Novel Thyroid Transcription Factor 1 Mutation

, , , , , ,

Journal: Journal of Child Neurology - JCN , vol. 27, no. 1, pp. 68-73, 2012

Changes in cognitive functions of students in the transitional period from elementary school to junior high school (Citations: 3)

, , , , ,

Journal: Brain & Development - BRAIN DEVELOP , vol. 33, no. 5, pp. 412-420, 2011

Relationship between cognitive function and prevalence of decrease in intrinsic academic motivation in adolescents (Citations: 1)

, , , ,

Journal: Behavioral and Brain Functions - BEHAV BRAIN FUNCT , vol. 7, no. 1, pp. 4-11, 2011

Subclinical hypothyroidism in childhood (Citations: 1)

Journal: Archives of Disease in Childhood - ARCH DIS CHILD , vol. 96, no. 3, pp. 280-284, 2011

Two novel mutations in PEO1 (Twinkle) gene associated with chronic external ophthalmoplegia

, , , , , , , , , , , http://academic.research.microsoft.com/io.ashx?type=5&id=49100733&selfId1=21504260&selfId2=0&maxNumber=12&query=

Journal: Journal of The Neurological Sciences - J NEUROL SCI , vol. 308, no. 1, pp. 173-176, 2011

Comments


	View FAQ about top research areas and Fields of study

Co-authors (79)

Journals (13)

Keywords (34)

Noritaka Iwatani,Kumamoto University,Endocrinology,Genetics & Genealogy,Family Medicine

Publications (16) BibTeX | RIS | RefWorks Download

Learning and memorization impairment in childhood chronic fatigue syndrome manifesting as school phobia in Japan (Citations: 19)

Effects of exogenous melatonin on pituitary hormones in humans (Citations: 6)

Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure (Citations: 51)

Prevalence of GH1 Gene Deletion in Patients with Isolated Growth Hormone Deficiency in Japan (Citations: 2)

High-dose growth hormone (GH) treatment in prepubertal GH-deficient children (Citations: 5)

Citations (147 times by 143 publications)

Brain-Lung-Thyroid Disease: Clinical Features of a Kindred With a Novel Thyroid Transcription Factor 1 Mutation

Changes in cognitive functions of students in the transitional period from elementary school to junior high school (Citations: 3)

Relationship between cognitive function and prevalence of decrease in intrinsic academic motivation in adolescents (Citations: 1)

Subclinical hypothyroidism in childhood (Citations: 1)

Two novel mutations in PEO1 (Twinkle) gene associated with chronic external ophthalmoplegia

Publications (16)

BibTeX | RIS | RefWorks Download