M. Mikawa

发表

Confirmation of Down syndrome critical region by FISH analysis in a patient with add(21) (p11)

N. Niikawa, N. Matsumoto, M. Mikawa, 1995, American journal of medical genetics.

Atypical Familial Mediterranean Fever in a Japanese Boy with Heterozygous MEFV p.Ser503Cys Exon 5 Variant

S. Takezaki, Takeru Goto, M. Mikawa, 2021, Case reports in pediatrics.

Congenital Dermatofibrosarcoma Protuberans in a Newborn Infant With a Massive Back Tumor: Favorable Effects of Oral Imatinib on the Control of Residual Tumor Growth

Kunihiko Kobayashi, D. Suzuki, Keita Morioka, 2011, Journal of pediatric hematology/oncology.

A One-Year-Old Girl With Human Parvovirus B19 Infection and Hypocomplementemia Mimicking Incomplete Kawasaki Disease

M. Mikawa, Tomonobu Sato, S. Ishikawa, 2022, Journal of medical cases.

ENDOTOXIN CLEARANCE BY EXCHANGE BLOOD TRANSFUSION IN SEPTIC SHOCK NEONATES

H. Togari, Y. Wada, M. Hagisawa, 1983, Acta paediatrica Scandinavica.

Anarchy in the Unity: Compositional and Aesthetic Tensions in Mauricio Kagel's Antithese für einen Darsteller mit elektronischen und öffentlichen Klängen (1962)

M. Mikawa, 2012 .

The impact of COVID‐19 pandemic on pediatric hospitalization in Kitami, Japan

M. Mikawa, Tomonobu Sato, S. Ishikawa, 2021, Pediatrics international : official journal of the Japan Pediatric Society.

Hirschsprung disease, unusual face, mental retardation, epilepsy, and congenital heart disease: Goldberg-Shprintzen syndrome.

H. Tanaka, M. Mikawa, J. Ito, 1993, Pediatric neurology.

Two-Site “Simultaneous” Immunoassay with Monoclonal Antibodies for the Determination of Surfactant Apoproteins in Human Amniotic Fluid

Y. Fukada, Y. Kuroki, Hiroki Takahashi, 1985, Pediatric Research.

An Immunoglobulin A Vasculitis Case Without Skin Symptoms Complicated With Severe Abdominal Symptoms

Kota Watanabe, M. Mikawa, Tomonobu Sato, 2022, Journal of Medical Cases.

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

Y. Fukushima, N. Niikawa, N. Matsumoto, 2008, Clinical dysmorphology.

Another observation of Langer-type sponastrime dysplasia variant.

Y. Fukushima, G. Nishimura, Y. Fukushima, 1998, American journal of medical genetics.

Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form: Clinical course and phenotypic variations in four patients

Y. Fukushima, T. Shiihara, S. Ikegawa, 2002, American journal of medical genetics. Part A.