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Kiyoshi Imaizumi

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Kiyoshi Imaizumi; Junko Kimura; Mari Matsuo; Kenji Kurosawa; Mitsuo Masuno; Norio Niikawa; Yoshikazu Kuroki
Sotos syndrome associated with a de novo balanced reciprocal translocation t(5;8)(q35;q24.1).
Keisuke Kato; Kiyoshi Matsui; M Hoshino; Motoyoshi Kawataki; Makiko Ohyama; Yasufumi Itani; Kiyoshi Imaizumi; Hisato Kigasawa
Tumor cell lysis syndrome resulting from transient abnormal myelopoiesis in a neonate with Down's syndrome.
Kiyoshi Imaizumi
[Toriello-Carey syndrome].

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2002: Kiyoshi Imaizumi; Junko Kimura; Mari Matsuo; Kenji Kurosawa; Mitsuo Masuno; Norio Niikawa; Yoshikazu Kuroki
Sotos syndrome associated with a de novo balanced reciprocal translocation t(5;8)(q35;q24.1).
American journal of medical genetics 2002;107(1):58-60.
2001: Keisuke Kato; Kiyoshi Matsui; M Hoshino; Motoyoshi Kawataki; Makiko Ohyama; Yasufumi Itani; Kiyoshi Imaizumi; Hisato Kigasawa
Tumor cell lysis syndrome resulting from transient abnormal myelopoiesis in a neonate with Down's syndrome.
Pediatrics international : official journal of the Japan Pediatric Society 2001;43(1):84-6.
2001: Kiyoshi Imaizumi
[Toriello-Carey syndrome].
Ryōikibetsu shōkōgun shirīzu 2001;(34 Pt 2):737-8.
2001: Kiyoshi Imaizumi
[Gollop-Wolfgang syndrome].
Ryōikibetsu shōkōgun shirīzu 2001;(34 Pt 2):732-3.
2001: Kiyoshi Imaizumi
[Neonatal Marfan syndrome].
Ryōikibetsu shōkōgun shirīzu 2001;(34 Pt 2):277-8.
2001: Kiyoshi Imaizumi
[Goldberg-Shprintzen syndrome].
Ryōikibetsu shōkōgun shirīzu 2001;(33):761-2.
2001: Kiyoshi Imaizumi
[Chromosome 15].
Ryōikibetsu shōkōgun shirīzu 2001;(33):422-4.
2001: Kiyoshi Imaizumi
[Chromosome 14].
Ryōikibetsu shōkōgun shirīzu 2001;(33):419-21.
2001: Kiyoshi Imaizumi
[Chromosome 12].
Ryōikibetsu shōkōgun shirīzu 2001;(33):414-6.
2001: Kiyoshi Imaizumi
[Chromosome 11].
Ryōikibetsu shōkōgun shirīzu 2001;(33):411-3.
2001: Kiyoshi Imaizumi
[Chromosome 10].
Ryōikibetsu shōkōgun shirīzu 2001;(33):407-10.
2001: Kiyoshi Imaizumi
[Chromosome 9].
Ryōikibetsu shōkōgun shirīzu 2001;(33):403-6.
2001: Kiyoshi Imaizumi
[Chromosome 8].
Ryōikibetsu shōkōgun shirīzu 2001;(33):399-402.
2001: Kiyoshi Imaizumi
[Chromosome 7].
Ryōikibetsu shōkōgun shirīzu 2001;(33):396-8.
2001: Kiyoshi Imaizumi
[Chromosome 6].
Ryōikibetsu shōkōgun shirīzu 2001;(33):393-5.
2001: Kiyoshi Imaizumi
[Chromosome 3].
Ryōikibetsu shōkōgun shirīzu 2001;(33):384-7.
2001: Kiyoshi Imaizumi
[Chromosome 2].
Ryōikibetsu shōkōgun shirīzu 2001;(33):381-3.
2001: Kiyoshi Imaizumi
[Chromosome 1].
Ryōikibetsu shōkōgun shirīzu 2001;(33):377-80.
2001: Kiyoshi Imaizumi
[Wildervanck (cervico-oculo-acoustic) syndrome].
Ryōikibetsu shōkōgun shirīzu 2001;(33):361-2.
2001: Keisuke Kato; M Sugitani; Motoyoshi Kawataki; Makiko Ohyama; Noriko Aida; N Koga; Rieko Ijiri; Kiyoshi Imaizumi; Hisato Kigasawa; Yukichi Tanaka; Yasufumi Itani
Congenital dyserythropoietic anemia type 1 with fetal onset of severe anemia.
Journal of pediatric hematology/oncology 2001;23(1):63-6.
2000: Mitsuo Masuno; T Ishii; Yukichi Tanaka; Makiko Ohyama; Motoyoshi Kawataki; Junko Kimura; Kiyoshi Imaizumi; Yoshikazu Kuroki
De novo trisomy 16p11.2-qter: report of an infant.
American journal of medical genetics 2000;92(5):308-10.
2000: S Yamanaka; Yukichi Tanaka; Motoyoshi Kawataki; Rieko Ijiri; Kiyoshi Imaizumi; H Kurahashi
Chromosome 22q11 deletion complicated by dissecting pulmonary arterial aneurysm and jejunal atresia in an infant.
Archives of pathology & laboratory medicine 2000;124(6):880-2.
2000: Makiko Ohyama; Yasufumi Itani; Michiko Yamanaka; Kiyoshi Imaizumi; T Nishi; Rieko Ijiri; Yukichi Tanaka
Umbilical cord ulcer: a serious in utero complication of intestinal atresia.
Placenta 2000;21(4):432-5.
2000: Kiyoshi Imaizumi
[Aniridia-Wilms tumor association].
Ryōikibetsu shōkōgun shirīzu 2000;(30 Pt 5):327-8.
2000: Kiyoshi Imaizumi
[Partial trisomy 10q syndrome].
Ryōikibetsu shōkōgun shirīzu 2000;(30 Pt 5):325-6.
2000: Kiyoshi Imaizumi
[Marden-Walker syndrome].
Ryōikibetsu shōkōgun shirīzu 2000;(30 Pt 5):15-7.
2000: Kiyoshi Imaizumi
[Atelencephaly].
Ryōikibetsu shōkōgun shirīzu 2000;(28 Pt 3):413-5.
2000: Mitsuo Masuno; Kiyoshi Imaizumi; Noriko Aida; G Nishimura; Junko Kimura; Yoshikazu Kuroki
Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies: another observation.
Clinical dysmorphology 2000;9(1):59-60.
1999: Kiyoshi Imaizumi; Junko Kimura; Mitsuo Masuno; Yoshikazu Kuroki; T Nishi
Apple-peel intestinal atresia associated with balanced reciprocal translocation t(2;3)(q31.3;p24.2) mat.
American journal of medical genetics 1999;87(5):434-5.
1999: Kiyoshi Imaizumi; T Ishii; Junko Kimura; Mitsuo Masuno; Yoshikazu Kuroki
Association of microphthalmia with esophageal atresia: report of two new patients and review of the literature.
American journal of medical genetics 1999;87(2):180-2.
1999: Mitsuo Masuno; Kiyoshi Imaizumi; T Okada; M Adachi; G Nishimura; T Ishii; K Tachibana; Yoshikazu Kuroki
Young-Simpson syndrome: further delineation of a distinct syndrome with congenital hypothyroidism, congenital heart defects, facial dysmorphism, and mental retardation.
American journal of medical genetics 1999;84(1):8-11.
1998: Kiyoshi Imaizumi; T Ishii; Mitsuo Masuno; Yoshikazu Kuroki
Association of holoprosencephaly, ectrodactyly, cleft lip/cleft palate and hypertelorism: a possible third case.
Clinical dysmorphology 1998;7(3):213-6.
1997: Kiyoshi Imaizumi; Mitsuo Masuno; T Ishii; Yoshikazu Kuroki; N Okuzumi; Y Nakamura
Congenital scoliosis (hemivertebra) associated with de novo balanced reciprocal translocation, 46,XX,t(13;17)(q34;p11.2).
American journal of medical genetics 1997;73(3):244-6.
1997: Mitsuo Masuno; Kiyoshi Imaizumi; Y Fukushima; Yukichi Tanaka; T Ishii; M Nakamura; Yoshikazu Kuroki
Median cleft of upper lip and pedunculated skin masses associated with de novo reciprocal translocation 46,X,t(X;16)(q28;q11.2).
Journal of medical genetics 1997;34(11):952-4.