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Hironori Shibata
Observed name:
H Shibata
Institutions:
Keio University,
Kawasaki Municipal Hospital
Observed institutions:
Keio University,
Shizuoka City Shimizu Hospital,
Keio University Hospital,
Kawasaki Municipal Hospital,
Hino Municipal Hospital
ORCID:
0009-0001-8112-4800
Observed ORCID:
0009-0001-8112-4800
OpenAlex ID:
A5073467644
Genetic and functional analyses of TBX4 reveal novel mechanisms underlying pulmonary arterial hypertension
2022
·
Yu Yoshida
, Keiko Uchida
, et al.
·
Journal of Molecular and Cellular Cardiology
·
20
Acquired partial lipodystrophy with metabolic disease in children following hematopoietic stem cell transplantation: a report of two cases and a review of the literature
2019
·
Mayumi Hosokawa
, Hironori Shibata
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
20
Human Chorionic Gonadotropin Stimulation Test in Prepubertal Children with Micropenis Can Accurately Predict Leydig Cell Function in Pubertal or Postpubertal Adolescents
2015
·
Tomohiro Ishii
, Nobutake Matsuo
, et al.
·
Hormone Research in Paediatrics
·
17
A novel mutation in the ACAN gene in a family with autosomal dominant short stature and intervertebral disc disease
2020
·
Noboru Uchida
, Hironori Shibata
, et al.
·
Human Genome Variation
·
14
PDF
Meningitis and septicemia caused by nontypeable Haemophilus influenzae in a previously healthy 2-year-old girl
2011
·
Takao Ito
, Hironori Shibata
, et al.
·
Journal of Infection and Chemotherapy
·
14
PDF
Relapsing 6q24-related transient neonatal diabetes mellitus with insulin resistance: A case report
2020
·
Noboru Uchida
, Takuma Ohnishi
, et al.
·
Clinical Pediatric Endocrinology
·
8
PDF
Rapid Growth and Early Metastasis of Papillary Thyroid Carcinoma in an Adolescent Girl with Graves’ Disease
2018
·
Kazuhiro Shimura
, Hironori Shibata
, et al.
·
Hormone Research in Paediatrics
·
5
An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report
2022
·
Yuki Ishinoda
, Asuka Uto
, et al.
·
BMC Endocrine Disorders
·
4
PDF
A novel SOX10 variant in a Japanese girl with Waardenburg syndrome type 4C and Kallmann syndrome
2020
·
Junpei Hamada
, Fumihiro Ochi
, et al.
·
Human Genome Variation
·
4
PDF
Histological Changes in Autoimmune Hepatitis with Graves' Disease: A Child Case Report
2017
·
Mamiko Yamada
, Hironori Shibata
, et al.
·
Internal Medicine
·
4
PDF
A case of mature teratoma with a falsely high serum estradiol value measured with an immunoassay
2016
·
Mayumi Hosokawa
, Hironori Shibata
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
3
Pitfalls in estradiol measurement by electrochemiluminescence immunoassay: A case study of a prepubertal girl with a falsely elevated serum estradiol level
2024
·
Kyohei Furusawa
, Rumi Hachiya
, et al.
·
Clinical Pediatric Endocrinology
·
2
PDF
A novel missense variant of FGFR1 in a Japanese girl with Kallmann syndrome and holoprosencephaly
2022
·
Noboru Uchida
, Yusuke Mizuno
, et al.
·
Clinical Pediatric Endocrinology
·
2
PDF
An infant with congenital nephrogenic diabetes insipidus presenting with hypercalcemia and hyperphosphatemia
2021
·
Katsuo Tao
, Midori Awazu
, et al.
·
Endocrinology Diabetes and Metabolism Case Reports
·
2
PDF
Central precocious puberty in a boy with pseudohypoparathyroidism type Ia due to a novel GNAS mutation
2020
·
Ryosuke Kagami
, Takeshi Sato
, et al.
·
Clinical Pediatric Endocrinology
·
2
Severe hypertriglyceridemia during treatment of acute lymphoblastic leukemia associated with type III hyperlipoproteinemia
2017
·
Yuji Yamada
, Haruko Shima
, et al.
·
Pediatric Blood & Cancer
·
2
Two Japanese Infants With Hypothyroidism Following Exposure to Iodinated Contrast Media
2023
·
Kazuhiro Shimura
, Hironori Shibata
, et al.
·
JCEM Case Reports
·
1
PDF
Intracranial germinoma in the lateral ventricle with polydipsia and polyuria: a case report and literature review
2022
·
Yuki Kuranari
, Tomoru Miwa
, et al.
·
Child s Nervous System
·
1
Physical disability and quality-of-life burden in McCune-Albright syndrome: a nationwide survey in Japan
2026
·
Hironori Shibata
, Tomohiro Ishii
, et al.
·
Endocrine Journal
PDF
Characteristic external genitalia in male neonates with 5α-reductase deficiency
2024
·
Takeshi Munenaga
, Yosuke Ichihashi
, et al.
·
Endocrine Journal
PDF
Potential benefits of rapid genetic testing for germline WT1 in infants with bilateral renal tumors: A case report
2021
·
Haruna Yoshikawa
, Takeshi Sato
, et al.
·
Pediatric Blood & Cancer
Effect of Testosterone Enanthate Therapy on Adult Height, Genital Maturation, and Bone Mineral Density in Children and Adolescents with Male Hypogonadotropic Hypogonadism
2019
·
Hironori Shibata
, Tomohiro Ishii
, et al.
·
58th Annual ESPE Meeting (ESPE 2019)
Detection of somatic activating GNAS mutations in girls with isolated autonomous ovarian cyst by next generation sequencing
2016
·
Hironori Shibata
·
The Japanese Society for Pediatric Endocrinology
Monostotic Fibrous Dysplasia is a Single Disorder Caused by Somatic Mosaic Activating Mutations in GNAS
2016
·
Hironori Shibata
, Satoshi Narumi
, et al.
·
55th ESPE Meeting
Auxological Characteristics of Persistent Hyperinsulinemic Hypoglycemia at Birth
2015
·
Hironori Shibata
, Mamiko Yamada
, et al.
·
54th ESPE Meeting (ESPE 2015)
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Works count:
26
Citation count:
124
H-index:
6
I10-index:
5
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