Faculty Information - Miyamoto Noriko

（Last updated : 2024-04-01 16:42:06）

Miyamoto Noriko
Department School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine Department of Oral and Maxillofacial Surgery, Division of Oral and Maxillofacial

Position Assistant Professor

■ Published papers

1.	Original article	Innsbruck-style retromandibular anterior trans-parotid approach for condylar fractures: A retrospective review of 39 fractures 2023/06/21
2.	Case report	Unilateral Severe Condylar Resorption Following Internal Fixation in Bilateral Mandibular Condylar Fracture 2023/05/18
3.	Original article	The progress of medication-related osteonecrosis of the jaw with conservative initial treatment: A 12-year retrospective study of 129 patients 2021/04/21
4.	Case report	Mandibular Fracture in a Patient Taking a Direct Oral Anticoagulant 2020/10/08
5.	Case report	Refracture of the Mandibular Condyle in Epilepsy 2020
6.	Case report	Osteonecrosis of the jaw during lenvatinib therapy: A case report based on surgical management 2019/09/17
7.	Case report	Genial Tubercle Fracture 2018
8.	Original article	Characteristics of patients with benign partial epilepsy in infancy without PRRT2 mutations 2015/09
9.	Original article	An association of 19p13.2 microdeletions with Malan syndrome and Chiari malformation. 2015
10.	Original article	Single nucleotide variations in CLCN6 identified in patients with benign partial epilepsies in infancy and/or febrile seizures. 2015
11.	Original article	Growth patterns of patients with 1p36 deletion syndrome. 2014/05
12.	Original article	An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia, and behavioral abnormalities 2014/01
13.	Original article	Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4. 2014
14.	Original article	Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA. 2014
15.	Original article	A novel homozygous mutation of GJC2 derived from maternal uniparental disomy in a female patient with Pelizaeus-Merzbacher-like disease. 2013/07
16.	Case report	De novo triplication of 11q12.3 in a patient with developmental delay and distinctive facial features. 2013/03
17.	Original article	A novel nucleotide mutation leading to a recurrent amino acid alteration in SH3BP2 in a patient with cherubism. 2013
18.	Original article	Microdeletions of 5.5Mb (4q13.2-q13.3) and 4.1Mb (7p15.3-p21.1) associated with a saethre-chotzen-like phenotype, severe intellectual disability, and autism. 2013
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■ Academic conference presentation

1.	Innsbruck-style retromandibular anterior trans-parotid approach for condylar fractures: Experience in Tokyo 2024/02/02
2.	Surgical complications with internal fixation of mandibular condylar fractures using retro-mandibular anterior trans-parotid (RAT/ Innsbruck) approach 2023/11/07
3.	A case of ectopic calcification found with inflammation 2021/11/12
4.	Characteristics of the patients with benign partial epilepsy in infancy due to PRRT2 mutations 2014/11