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Kiyoshi Kikkawa
Observed names:
K Kikkawa,
K. Kikkawa,
KIKKAWA, Kiyoshi,
Kiyoshi KIKKAWA,
Phd Kiyoshi Kikkawa
Institution:
Kochi Health Sciences Center
Observed institutions:
Shandong University,
Okayama University,
Fukuoka University,
RIKEN,
Kochi Municipal Central Hospital,
Qilu Hospital of Shandong University,
Kochi Health Sciences Center,
Nagoya University,
Amrita Vishwa Vidyapeetham
show all 9
OpenAlex ID:
A5036028319
Regional mapping of catalase and Wilms tumor?aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305?p1306
1984
·
K. Narahara
, K. Kikkawa
, et al.
·
Human Genetics
·
82
Probable assignment of soluble isocitrate dehydrogenase (IDH1) to 2q33.3
1985
·
K. Narahara
, S. Kimura
, et al.
·
Human Genetics
·
63
Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: Karyotype‐phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3
1990
·
Kouji Narahara
, Kiyoshi Kikkawa
, et al.
·
American Journal of Medical Genetics
·
59
Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)
2021
·
Mari Minatogawa
, Ai Unzaki
, et al.
·
Journal of Medical Genetics
·
44
PDF
Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures
2009
·
H. Kurahashi
, J. -w. Wang
, et al.
·
Neurology
·
36
Interstitial deletion of the long arm of chromosome 2: A case report and review of the literature
1985
·
Yukio Takahashi
, Kouji Narahara
, et al.
·
The Japanese Journal of Human Genetics
·
33
The critical monosomic segment involved in 4p- syndrome: A high-resolution banding study on five inherited cases
1984
·
Kouji Narahara
, Yusuke Himoto
, et al.
·
The Japanese Journal of Human Genetics
·
21
Assignment of ABO locus to 9q31.3→qter by study of a family in which an intrachromosomal shift involving chromosome 9 is segregating
1986
·
Kouji Narahara
, Yukio Takahashi
, et al.
·
The Japanese Journal of Human Genetics
·
20
Craniosynostosis and hemizygosity for D7S135 caused by a de novo and apparently balanced t(6;7) translocation
1994
·
Kazushiro Tsuji
, Kouji Narahara
, et al.
·
American Journal of Medical Genetics
·
18
Duplication of 2p25: confirmation of the assignment of soluble acid phosphatase (ACP1) locus to 2p25
1985
·
Y. Wakita
, K. Narahara
, et al.
·
Human Genetics
·
18
Is loss of band 7p21 really critical for manifestation of craniosynostosis in 7p‐?
1993
·
Kiyoshi Kikkawa
, Kouji Narahara
, et al.
·
American Journal of Medical Genetics
·
17
45,X/46,X,idic(Yq) mosaicism: Clinical, cytogenetic, and molecular studies in four individuals
1998
·
Michio Teraoka
, Koji Narahara
, et al.
·
American Journal of Medical Genetics
·
16
Role of Class III phosphoinositide 3‐kinase in the brain development: possible involvement in specific learning disorders
2016
·
Yutaka Inaguma
, Ayumi Matsumoto
, et al.
·
Journal of Neurochemistry
·
15
Verification of risk scores to predict i.v. immunoglobulin resistance in incomplete Kawasaki disease
2015
·
Kiichiro Kanamitsu
, Hisako Kakimoto
, et al.
·
Pediatrics International
·
13
De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies
1992
·
Yoshiharu Wakita
, Kouji Narahara
, et al.
·
Human Genetics
·
13
Pallister-Killian syndrome: Cytogenetic and biochemical studies
1988
·
Kouji Narahara
, Yoshiharu Wakita
, et al.
·
The Japanese Journal of Human Genetics
·
12
Reproductive risk of paracentric inversion carriers: Report of two unrelated cases with paracentric inversion of the long ARM of chromosome 3
1985
·
Ryozo Kasai
, Kouji Narahara
, et al.
·
The Japanese Journal of Human Genetics
·
9
Ventriculoperitoneal shunt outcomes among infants.
2015
·
Hidehiko Maruyama
, Yusei Nakata
, et al.
·
PubMed
·
8
Distal 14q trisomy syndrome in two siblings: Further delineation of its phenotype
1988
·
Yoshiharu Wakita
, Kouji Narahara
, et al.
·
The Japanese Journal of Human Genetics
·
8
Minimally Conjoined Omphalopagus Twins with a Body Stalk Anomaly
2015
·
Takeshi Inagaki
, Yusei Nakata
, et al.
·
American Journal of Perinatology Reports
·
6
PDF
Determination of orotic acid in urine and serum by isotachophoretic analysis
1990
·
Tomoki Takechi
, Hiroshi Wakiguchi
, et al.
·
Journal of Chromatography B Biomedical Sciences and Applications
·
5
Positive Minimal Residual Disease of FLT3-ITD before Hematopoietic Stem Cell Transplantation Resulted in a Poor Prognosis of an Acute Myeloid Leukemia.
2017
·
Yuka Iwasaki
, Rituo Nishiuchi
, et al.
·
PubMed
·
4
PDF
Importance of Milk Expression for Preterm Infants.
2016
·
Hidehiko Maruyama
, Yusei Nakata
, et al.
·
PubMed
·
4
PDF
Reliability of a rapid test for the clinical diagnosis of influenza A/H1N1 2009
2012
·
Daisuke Harada
, Ritsuo Nishiuchi
, et al.
·
Scandinavian Journal of Infectious Diseases
·
4
Gene dosage effects for coagulation factors XII (F12) and XIII subunit a (F13A) in a case with partial monosomy 6p resulting from a maternal pericentric inversion of chromosome 6
1987
·
Kouji Narahara
, Yoshihito Seno
, et al.
·
The Japanese Journal of Human Genetics
·
4
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Works count:
33
Citation count:
540
H-index:
13
I10-index:
16
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