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1. 女性における腹圧性尿失禁：外科的治療後の症状の持続または再発 stress urinary incontinence in women persistent recurrent symptoms after surgical treatment
2. 女性における腹圧性尿失禁の外科的マネージメント：一次手術の選択 surgical management of stress urinary incontinence in women choosing a primary surgical procedure

English Journal

Clinical, developmental and molecular update on Cornelia de Lange syndrome and the cohesin complex: abstracts from the 2014 Scientific and Educational Symposium.

Kline AD1, Calof AL2,3, Lander AD3, Gerton JL4,5, Krantz ID6,7, Dorsett D8, Deardorff MA6,7, Blagowidow N1, Yokomori K9, Shirahige K10, Santos R3, Woodman J11, Megee PC11, O'Connor JT12,13, Egense A14, Noon S6, Belote M15, Goodban MT16, Hansen BD17, Timmons JG18, Musio A19, Ishman SL20, Bryan Y21, Wu Y6, Bettini LR22, Mehta D6, Zakari M4, Mills JA6, Srivastava S13, Haaland RE23.
American journal of medical genetics. Part A.Am J Med Genet A.2015 Jun;167(6):1179-92. doi: 10.1002/ajmg.a.37056. Epub 2015 Apr 21.
Cornelia de Lange Syndrome (CdLS) is the most common example of disorders of the cohesin complex, or cohesinopathies. There are a myriad of clinical issues facing individuals with CdLS, particularly in the neurodevelopmental system, which also have implications for the parents and caretakers, involv
PMID 25899772

Rhythms and blues: modulation of oscillatory synchrony and the mechanism of action of antidepressant treatments.

Leuchter AF1, Hunter AM, Krantz DE, Cook IA.
Annals of the New York Academy of Sciences.Ann N Y Acad Sci.2015 May;1344:78-91. doi: 10.1111/nyas.12742. Epub 2015 Mar 23.
Treatments for major depressive disorder (MDD) act at different hierarchical levels of biological complexity, ranging from the individual synapse to the brain as a whole. Theories of antidepressant medication action traditionally have focused on the level of cell-to-cell interaction and synaptic neu
PMID 25809789

12p microRNA expression in fibroblast cell lines from probands with Pallister-Killian syndrome.

Izumi K1, Zhang Z, Kaur M, Krantz ID.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology.Chromosome Res.2014 Dec;22(4):453-61. doi: 10.1007/s10577-014-9431-y. Epub 2014 Jul 1.
Pallister-Killian syndrome is a multisystem sporadic genetic diagnosis characterized by facial dysmorphia, variable developmental delay and intellectual impairment, hypotonia, seizures, diaphragmatic hernia, and other systemic abnormalities. Pallister-Killian syndrome is typically caused by the pres
PMID 24981202