Sakazume S - Search Results

1

Corrigendum to "Validation of auxological reference values for Japanese children with Noonan syndrome and comparison with growth in children with Turner syndrome".

Isojima T, Sakazume S, Hasegawa T, Ogata T, Nakanishi T, Nagai T, Yokoya S. Isojima T, et al. Among authors: sakazume s. Clin Pediatr Endocrinol. 2022;31(3):210. doi: 10.1297/cpe.31.210. Epub 2022 Jul 13. Clin Pediatr Endocrinol. 2022. PMID: 35928385 Free PMC article.

2

[Chromosomal analysis in congenital malformation syndromes].

Sakazume S, Nagai T. Sakazume S, et al. Nihon Rinsho. 1999 Dec;57 Suppl:648-50. Nihon Rinsho. 1999. PMID: 10778212 Review. Japanese. No abstract available.

3

Genetic evidence for a novel gene(s) involved in urogenital development on 10q26.

Ogata T, Muroya K, Sasagawa I, Kosho T, Wakui K, Sakazume S, Ito K, Matsuo N, Ohashi H, Nagai T. Ogata T, et al. Among authors: sakazume s. Kidney Int. 2000 Dec;58(6):2281-90. doi: 10.1046/j.1523-1755.2000.00412.x. Kidney Int. 2000. PMID: 11115062 Free article.

4

Postnatal overgrowth by 15q-trisomy and intrauterine growth retardation by 15q-monosomy due to familial translocation t(13;15): dosage effect of IGF1R?

Nagai T, Shimokawa O, Harada N, Sakazume S, Ohashi H, Matsumoto N, Obata K, Yoshino A, Murakami N, Murai T, Sakuta R, Niikawa N. Nagai T, et al. Among authors: sakazume s. Am J Med Genet. 2002 Nov 22;113(2):173-7. doi: 10.1002/ajmg.10717. Am J Med Genet. 2002. PMID: 12407708

5

Fifty microdeletions among 112 cases of Sotos syndrome: low copy repeats possibly mediate the common deletion.

Kurotaki N, Harada N, Shimokawa O, Miyake N, Kawame H, Uetake K, Makita Y, Kondoh T, Ogata T, Hasegawa T, Nagai T, Ozaki T, Touyama M, Shenhav R, Ohashi H, Medne L, Shiihara T, Ohtsu S, Kato Z, Okamoto N, Nishimoto J, Lev D, Miyoshi Y, Ishikiriyama S, Sonoda T, Sakazume S, Fukushima Y, Kurosawa K, Cheng JF, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N. Kurotaki N, et al. Among authors: sakazume s. Hum Mutat. 2003 Nov;22(5):378-87. doi: 10.1002/humu.10270. Hum Mutat. 2003. PMID: 14517949

6

Bromocriptine treatment of prolactinoma restores growth hormone secretion and causes catch-up growth in a prepubertal child.

Sakazume S, Obata K, Takahashi E, Yoshino A, Murakami N, Sakuta R, Murai T, Nagai T. Sakazume S, et al. Eur J Pediatr. 2004 Aug;163(8):472-4. doi: 10.1007/s00431-004-1454-5. Epub 2004 May 25. Eur J Pediatr. 2004. PMID: 15160292

7

Cause of sudden, unexpected death of Prader-Willi syndrome patients with or without growth hormone treatment.

Nagai T, Obata K, Tonoki H, Temma S, Murakami N, Katada Y, Yoshino A, Sakazume S, Takahashi E, Sakuta R, Niikawa N. Nagai T, et al. Among authors: sakazume s. Am J Med Genet A. 2005 Jul 1;136(1):45-8. doi: 10.1002/ajmg.a.30777. Am J Med Genet A. 2005. PMID: 15937939

8

Membranoproliferative glomerulonephritis in a patient with X-linked agammaglobulinemia.

Yoshino A, Honda M, Kanegane H, Obata K, Matsukura H, Sakazume S, Katada Y, Miyawaki T, Ueda Y, Nagai T. Yoshino A, et al. Among authors: sakazume s. Pediatr Nephrol. 2006 Jan;21(1):36-8. doi: 10.1007/s00467-005-2029-z. Epub 2005 Nov 11. Pediatr Nephrol. 2006. PMID: 16550363

9

Growth hormone therapy and scoliosis in patients with Prader-Willi syndrome.

Nagai T, Obata K, Ogata T, Murakami N, Katada Y, Yoshino A, Sakazume S, Tomita Y, Sakuta R, Niikawa N. Nagai T, et al. Among authors: sakazume s. Am J Med Genet A. 2006 Aug 1;140(15):1623-7. doi: 10.1002/ajmg.a.31295. Am J Med Genet A. 2006. PMID: 16770808

10

De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment.

Kosho T, Sakazume S, Kawame H, Wakui K, Wada T, Okoshi Y, Mikawa M, Hasegawa T, Matsuura N, Niikawa N, Matsumoto N, Fukushima Y. Kosho T, et al. Among authors: sakazume s. Clin Dysmorphol. 2008 Jan;17(1):31-34. doi: 10.1097/MCD.0b013e3282f17688. Clin Dysmorphol. 2008. PMID: 18049078

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