Eiichi Kinoshita

Medicine · Health Sciences

18h-index1.1kcitations94works0.02yr avg
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Research Topics

Growth Hormone and Insulin-like Growth Factors(23), Sexual Differentiation and Disorders(12), Pituitary Gland Disorders and Treatments(8), Cancer, Hypoxia, and Metabolism(6), Genetics and Neurodevelopmental Disorders(6)

Publications93 total

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
Hormone Research in Paediatrics·2021· 14 cited
A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency
Journal of Human Genetics·2019· 18 citedOpen Access
Genetic background of hyperphenylalaninemia in <scp>Nagasaki</scp>, <scp>Japan</scp>
Pediatrics International·2016· 10 cited
Submicroscopic deletion involving the &lt;i&gt;fibroblast growth factor receptor 1&lt;/i&gt; gene in a patient with combined pituitary hormone deficiency
Endocrine Journal·2013· 18 citedOpen Access
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 with<i>LHX4</i>Deletion
The Journal of Clinical Endocrinology & Metabolism·2010· 52 cited
Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype
Endocrine Reviews·2010· 1 citedOpen Access
Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype
Endocrinology·2010
Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype
Molecular Endocrinology·2010· 8 citedOpen Access
Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype
The Journal of Clinical Endocrinology & Metabolism·2009· 107 cited
The Jewish‐type Cohen syndrome complicated with refractory bronchial asthma and depression
Pediatrics International·2005· 1 cited
Klippel‐Feil anomaly in a boy and Dubowitz syndrome with vertebral fusion in his brother: A new variant of Dubowitz syndrome?
American Journal of Medical Genetics Part A·2005· 5 cited
The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune?Albright syndrome
Journal of Bone and Mineral Metabolism·2005· 66 cited
GNAS1 Mutation Identified in Genomic DNA from Whole Blood of a Case with McCune-Albright Syndrome
Clinical Pediatric Endocrinology·2005Open Access
Treatment of gastric hemorrhage by pulverized omeprazole and antacid concomitant administration via a nasogastric tube
International Journal of Clinical Pharmacology and Therapeutics·2004· 1 cited
Two novel and one recurrent <i>PTPN11</i> mutations in LEOPARD syndrome
American Journal of Medical Genetics Part A·2004· 32 cited
Protein-Tyrosine Phosphatase, Nonreceptor Type 11 Mutation Analysis and Clinical Assessment in 45 Patients with Noonan Syndrome
The Journal of Clinical Endocrinology & Metabolism·2004· 111 citedOpen Access
Newly recognized syndrome of metaphyseal undermodeling, spondylar dysplasia, and overgrowth: Report of two adolescents and a child
American Journal of Medical Genetics Part A·2004· 7 cited
Renal tubular dysgenesis complicated with severe cranium hypoplasia
Pediatrics International·2004· 4 cited
Persistent hepatitis associated with chronic active epstein-barr virus infection
The Pediatric Infectious Disease Journal·2004· 30 cited
1 Molecular genetics, diagnosis and management of adrenal diseases in childhood
Nagasaki University's Academic Output SITE (Nagasaki University)·2003Open Access
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Frequent Co-authors

Hiroyuki Moriuchi(11), Tadashi Matsumoto(11), Tsutomu Ogata(9), Tatsuro Kondoh(8), Tomonobu Hasegawa(6), Sumito Dateki(6), Masaaki Yoshimoto(6), John S. Parks(5), Yoshiro Tsuji(5), Noboru Takamura(4), Shunichi Yamashita(4), Toshiro Nagai(4), Toshiaki Tanaka(4), Toshihiro Tajima(4), Maki Fukami(4), Norio Niikawa(4), Milton R. Brown(3), Valentina Peterkova(3), Susumu Yokoya(3), Koji Muroya(3)