S. Yokoyama

发表

Chromosomal aberration in lipoblastoma: a case with 46,XX,ins(8;6)(q11.2;q13q27).

T. Shiihara, K. Hayasaka, E. Saitoh, 1997, Cancer genetics and cytogenetics.

Microangiopathic hemolytic anemia and thrombocytopenia in a child with atrial septal defect and pulmonary hypertension.

M. Nakasato, S. Sato, K. Hayasaka, 1997, The Tohoku journal of experimental medicine.

Coronary fibromuscular dysplasia presenting as sudden infant death.

M. Imamura, K. Kikuchi, S. Yokoyama, 1997, Archives of pathology & laboratory medicine.

Prenatal diagnosis of GM1-gangliosidosis: Biochemical manifestations in fetal tissues

T. Kudoh, S. Yokoyama, T. Nakao, 1978, Human Genetics.

Severe Bleeding Tendency in a Patient With Bernard‐Soulier Syndrome Associated With a Homozygous Single Base Pair Deletion in the Gene Coding for the Human Platelet Glycoprotein Ibα

Tomohiro Hayashi, K. Hayasaka, T. Hayashi, 1998, Journal of pediatric hematology/oncology.

Muscular dystrophy associated with extra-abdominal desmoid tumor showing aberrant chromosome 1 [46,XX,add(1)(p36)].

I. Nonaka, K. Hayasaka, Y. Takahashi, 1998, American journal of medical genetics.

Novel mutations of the glutaryl-CoA dehydrogenase gene in two Japanese patients with glutaric aciduria type I.

K. Hayasaka, S. Yamaguchi, T. Ohura, 1998, American journal of medical genetics.

Genetic polymorphisms of bone marrow stromal cell antigen-1 (BST-1/CD157): implications for immune/inflammatory dysfunction in neuropsychiatric disorders

S. Yokoyama, 2023, Frontiers in Immunology.

Severe hypertension and cardiac failure associated with neuroblastoma: a case report.

K. Hayasaka, T. Wakabayashi, S. Yokoyama, 1996, Journal of pediatric surgery.