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Eiichi Kinoshita
Observed names:
E Kinoshita,
E. KINOSHITA,
E. Kinoshita,
E.-i. Kinoshita,
EI-ICHI KINOSHITA,
EIICHI KINOSHITA,
Ei-Ichi Kinoshita,
Ei-ichi Kinoshita,
Eiichi KINOSHITA,
Ei‐ichi Kinoshita
show all 10
Observed institutions:
Kurume University,
Emory University,
Keio University,
Nishida Hospital,
Kyoto University Hospital,
Nagasaki University,
Tagawa Municipal Hospital,
Tagawa Hospital,
Kumamoto Kinoh Hospital,
Nagoya University
show all 10
OpenAlex ID:
A5110062981
Compound Heterozygous Deletion of the PROP-1 Gene in Children with Combined Pituitary Hormone Deficiency
1998
·
Q. Fofanova
, N. Takamura
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
132
Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype
2009
·
Sumito Dateki
, Kitaro Kosaka
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
113
Protein-Tyrosine Phosphatase, Nonreceptor Type 11 Mutation Analysis and Clinical Assessment in 45 Patients with Noonan Syndrome
2004
·
Rie Yoshida
, Tomonobu Hasegawa
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
111
MR Imaging of the Pituitary Gland in Children and Young Adults with Congenital Combined Pituitary Hormone Deficiency Associated with PROP1 Mutations
2000
·
Olga Fofanova
, Noboru Takamura
, et al.
·
American Journal of Roentgenology
·
64
The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune?Albright syndrome
2005
·
Takehisa Yamamoto
, Yasuo Imanishi
, et al.
·
Journal of Bone and Mineral Metabolism
·
63
Mutation and Gene Copy Number Analyses of Six Pituitary Transcription Factor Genes in 71 Patients with Combined Pituitary Hormone Deficiency: Identification of a Single Patient withLHX4Deletion
2010
·
Sumito Dateki
, Maki Fukami
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
55
Growth retardation due to idiopathic growth hormone deficiencies: MR findings in 24 patients
1992
·
M. Ochi
, M. Morikawa
, et al.
·
Pediatric Radiology
·
36
Two novel and one recurrent PTPN11 mutations in LEOPARD syndrome
2004
·
Rie Yoshida
, Toshiro Nagai
, et al.
·
American Journal of Medical Genetics Part A
·
33
Usefulness of Renal Ultrasonography for Assessment of Severity and Course of Acute Tubular Necrosis
1984
·
Gakuji Nomura
, Eiichi Kinoshita
, et al.
·
Journal of Clinical Ultrasound
·
33
No evidence of PEG1MEST gene mutations in Silver‐Russell syndrome patients
2001
·
Shin Kobayashi
, Hiraku Uemura
, et al.
·
American Journal of Medical Genetics
·
31
Mutations in intron 3 of GH‐1 gene associated with isolated GH deficiency type II in three Japanese families
1999
·
Takashi Kamijo
, Yoshitaka Hayashi
, et al.
·
Clinical Endocrinology
·
29
Molecular analysis of type II 3 -hydroxysteroid dehydrogenase gene in Japanese patients with classical 3 -hydroxysteroid dehydrogenase deficiency
1995
·
T. Tajima
, K. Fujieda
, et al.
·
Human Molecular Genetics
·
28
Pit-1 and hypopituitarism
1993
·
John S. Parks
, Ei-Ichi Kinoshita
, et al.
·
Trends in Endocrinology and Metabolism
·
27
Genetics of Growth Hormone Gene Expression
1993
·
John S. Parks
, Hussein Abdul-Latif
, et al.
·
Hormone Research
·
27
DAX-1 Gene Mutations and Deletions in Japanese Patients with Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism
1997
·
Ei-ichi Kinoshita
, Ei-ichi Kinoshita
, et al.
·
Hormone Research
·
25
Submicroscopic deletion involving the fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency
2013
·
Maki Fukami
, Manami Iso
, et al.
·
Endocrine Journal
·
21
PDF
A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency
2019
·
Sumito Dateki
, Satoshi Watanabe
, et al.
·
Journal of Human Genetics
·
20
Rapid detection of a point mutation in thyroid-stimulating hormoneβ-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency
1991
·
Ryogo Mori
, Tomoko Sawai
, et al.
·
The Japanese Journal of Human Genetics
·
19
Novel mutations of the ACTH receptor gene in a female adult patient with adrenal unresponsiveness to ACTH
2000
·
Tomohiro Ishii
, Tsutomu Ogata
, et al.
·
Clinical Endocrinology
·
18
A Case of Farber Disease
1992
·
Takehisa Fujiwaki
, Sumiko Hamanaka
, et al.
·
Pediatrics International
·
18
Mental Retardation in a Boy with Congenital Adrenal Hypoplasia: A Clue to Contiguous Gene Syndrome Involving DAX1 and IL1RAPL
2003
·
RIE SASAKI
, YASUJI INAMO
, et al.
·
Endocrine Journal
·
16
PDF
The Boy:Girl Ratio of Children Diagnosed with Growth Hormone Deficiency-Induced Short Stature Is Associated with the Boy:Girl Ratio of Children Visiting Short Stature Clinics
2021
·
Toshiaki Tanaka
, Shun Soneda
, et al.
·
Hormone Research in Paediatrics
·
15
Hearing impairment, undescended testis, circumferential skin creases, and mental handicap (HITCH) syndrome: A case report
2003
·
Tatsuro Kondoh
, Jiro Eguchi
, et al.
·
American Journal of Medical Genetics Part A
·
14
Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma
1994
·
Tadashi Matsumoto
, Ei-ichi Kinoshita
, et al.
·
The Japanese Journal of Human Genetics
·
14
PDF
Genetic background of hyperphenylalaninemia in Nagasaki , Japan
2016
·
Sumito Dateki
, Satoshi Watanabe
, et al.
·
Pediatrics International
·
11
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Works count:
79
Citation count:
1,125
H-index:
19
I10-index:
27
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