Makiko Ōsawa - Concepedia

Author

Makiko Ōsawa

Tokyo Women's Medical University

Also Known As

M Osawa, MAKIKO OSAWA, Makiko OSAWA, Makiko Osawa, Makiko Ōsawa

287

Publications

7.1K

Citations

H-Index

152

Concepts

All Affiliations

Tokyo Women's Medical University National Center of Neurology and Psychiatry National Epilepsy Center Tottori University

MŌ

About

Makiko Ōsawa is an author at Tokyo Women's Medical University specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	69	2.4K
2	Social Sciences	10	10	343
3	Health Sciences	7	7	212
4	Public Health	5	5	183
5	Natural Sciences	1	1	41

Makiko Ōsawa

124

Publications

6.3K

Citations

H-Index

Page 1

	Year	Citations
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy Kazuhiro Kobayashi, Yutaka Nakahori, Masashi Miyake, Nature Degenerative SpineDegenerative DiseaseOrthopaedic SurgeryNeuromusculoskeletal DisorderAncient Retrotransposal Insertion	1998	801
Congenital progressive muscular dystrophy of the fukuyama type — clinical, genetic and pathological considerations — Yukio Fukuyama, Makiko Ōsawa, Haruko Suzuki Brain and Development Rare DiseasesMendelian DisorderPathological ConsiderationsMedicineFukuyama Type —	1981	471
Mutations in EFHC1 cause juvenile myoclonic epilepsy Toshimitsu Suzuki, Antonio V. Delgado‐Escueta, Kripamoy Aguan, Nature Genetics Disease Gene IdentificationGeneticsNeuroscienceGenetic Disorder	2004	370
Long-Term Outcomes of Pediatric Moyamoya Disease Monitored to Adulthood Tomoichi Imaizumi, Kitami Hayashi, Kayoko Saito, Pediatric Neurology MoxibustionDiagnosisPediatricsLong-term OutcomesEpidemiology	1998	179
Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness Terumi Murakami, Yukiko Hayashi, S. Noguchi, Annals of Neurology	2006	148
A modified Atkins diet is promising as a treatment for glucose transporter type 1 deficiency syndrome Yasushi Ito, Hirokazu Oguni, Susumu Ito, Developmental Medicine & Child Neurology	2011	134
Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on Chromosome 7q11.23 Hamao Hirota, Rumiko Matsuoka, Xiao–Ning Chen, Genetics in Medicine Chromosome 7Q11.23Genetic DisorderGeneticsPsychiatric GeneticsNeurogenetics	2003	123
Beta-Blocker Therapy for Cardiac Dysfunction in Patients With Muscular Dystrophy Hidemi Kajimoto, Keiko Ishigaki, Kenichi Okumura, Circulation Journal	2006	118
Mouse with Nav1.1 haploinsufficiency, a model for Dravet syndrome, exhibits lowered sociability and learning impairment Susumu Ito, Ikuo Ogiwara, Kazuyuki Yamada, Neurobiology of Disease Knockout MouseDravet SyndromeDevelopmental BiologyMolecular NeuroscienceGenetic Disorder	2012	117
Long‐Term Prognosis of Lennox‐Gastaut Syndrome Hirokazu Oguni, Kitami Hayashi, Makiko Ōsawa Epilepsia	1996	115

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