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1. 黒人における高血圧合併症 hypertensive complications in blacks
2. 小児における血小板減少症の原因 causes of thrombocytopenia in children
3. 遺伝性腎炎（アルポート症候群）の臨床症状、診断および治療 clinical manifestations diagnosis and treatment of hereditary nephritis alport syndrome
4. 慢性腎臓病の疫学 epidemiology of chronic kidney disease
5. 巣状分節性糸球体硬化症の疫学、分類、および病因 epidemiology classification and pathogenesis of focal segmental glomerulosclerosis

English Journal

Kinetics and mechanics of clot contraction are governed by the molecular and cellular composition of the blood.

Tutwiler V1, Litvinov RI2, Lozhkin AP3, Peshkova AD3, Lebedeva T4, Ataullakhanov FI5, Spiller KL6, Cines DB4, Weisel JW2.
Blood.Blood.2016 Jan 7;127(1):149-59. doi: 10.1182/blood-2015-05-647560. Epub 2015 Nov 24.
Platelet-driven blood clot contraction (retraction) is thought to promote wound closure and secure hemostasis while preventing vascular occlusion. Notwithstanding its importance, clot contraction remains a poorly understood process, partially because of the lack of methodology to quantify its dynami
PMID 26603837

Natural IgM Blockade Limits Infarct Expansion and Left Ventricular Dysfunction in a Swine Myocardial Infarct Model.

Sihag S1, Haas MS1, Kim KM1, Guerrero JL1, Beaudoin J1, Alicot EM1, Schuerpf F1, Gottschall JD1, Puro RJ1, Madsen JC1, Sachs DH1, Newman W1, Carroll MC1, Allan JS1.
Circulation. Cardiovascular interventions.Circ Cardiovasc Interv.2016 Jan;9(1):e002547. doi: 10.1161/CIRCINTERVENTIONS.115.002547.
BACKGROUND: Acute coronary syndrome is the leading cause of mortality worldwide. However, treatment of acute coronary occlusion inevitably results in ischemia-reperfusion injury. Circulating natural IgM has been shown to play a significant role in mouse models of ischemia-reperfusion injury. A highl
PMID 26671971

Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.

Verver EJ1, Topsakal V, Kunst HP, Huygen PL, Heller PG, Pujol-Moix N, Savoia A, Benazzo M, Fierro T, Grolman W, Gresele P, Pecci A.
Ear and hearing.Ear Hear.2016 Jan-Feb;37(1):112-20. doi: 10.1097/AUD.0000000000000198.
OBJECTIVES: MYH9-related disease (MYH9-RD) is an autosomal- dominant disorder deriving from mutations in MYH9, the gene for the nonmuscle myosin heavy chain (NMMHC)-IIA. MYH9-RD has a complex phenotype including congenital features, such as thrombocytopenia, and noncongenital manifestations, namely
PMID 26226608