Masahiro Kikuchi

发表

An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

Alexander E. Lopez, Aaron M. King, Andrew L Blumenfeld, 2021, Journal of hepatology.

Alterations of effector cell molecule expression on neutrophils in granulocyte colony‐stimulating factor‐producing tumour

A. Ohsaka, Y. Itoh, K. Endo, 1995, British journal of haematology.

A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study.

O. Ohara, T. Awaya, T. Heike, 2014, Rheumatology.

POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33

Y. Maehara, M. Honda, O. Yokosuka, 2019, Scientific Reports.

X chromosome contribution to the genetic architecture of primary biliary cholangitis.

Aaron M. King, Elizabeth G. Atkinson, K. Siminovitch, 2021, Gastroenterology.

Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy

N. Matsumoto, K. Ogata, Makoto Kobayashi, 2021, Clinical genetics.

Genome‐wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population

Y. Maehara, K. Chayama, M. Honda, 2017, Human molecular genetics.

Bickerstaff's Brainstem Encephalitis Associated With IgG Anti-GQ1b Antibody Subsequent to Mycoplasma pneumoniae Infection: Favorable Response to Immunoadsorption Therapy

N. Yuki, H. Iwamoto, H. Iwamoto, 1997, Journal of child neurology.

POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33

Y. Maehara, M. Honda, O. Yokosuka, 2019, Scientific Reports.

Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene

R. Skoda, A. Ohsaka, N. Ghilardi, 1999, British journal of haematology.

Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency

Kyoko Takano, H. Osaka, R. Weiss, 2021, Thyroid : official journal of the American Thyroid Association.

Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases

J. Takanashi, T. Shiihara, M. Mizuguchi, 2011, Brain and Development.

Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581]

Alexander E. Lopez, Aaron M. King, Andrew L Blumenfeld, 2021, Journal of hepatology.

Clinical and Radiological Features of Rotavirus Cerebellitis

A. Barkovich, J. Takanashi, M. Kikuchi, 2010, American Journal of Neuroradiology.

Widening spectrum of a reversible splenial lesion with transiently reduced diffusion.

A. Barkovich, J. Takanashi, T. Shiihara, 2006, AJNR. American journal of neuroradiology.

Brief report: severe infectious mononucleosis-like syndrome and primary human herpesvirus 6 infection in an adult.

K. Akashi, Sachiko Hara, M. Harada, 1993, The New England journal of medicine.

Evolution of severe aplastic anemia to myelodysplasia with monosomy 7 following granulocyte colony-stimulating factor, erythropoietin and high-dose methylprednisolone combination therapy.

A. Ohsaka, M. Kikuchi, Y. Imai, 1995, Internal medicine.