X. Li

发表

Diagnosis and molecular analysis of an atypical case of holocarboxylase synthetase deficiency

N. Shimizu, E. Holme, M. Hiratsuka, 2000, European Journal of Pediatrics.

Identification and characterization of mutations in patients with holocarboxylase synthetase deficiency

T. Suormala, E. R. Baumgartner, Xia Li, 1999, Human Genetics.

Enzymatic diagnosis of holocarboxylase synthetase deficiency using apo-carboxyl carrier protein as a substrate.

Xia Li, H. Kondo, Y. Suzuki, 1996, Clinica chimica acta; international journal of clinical chemistry.

Childhood-onset of primary Sjogren syndromePhenotypic characterization at diagnosis of 158 children

A. Vissink, D. Isenberg, S. Bombardieri, 2020, medRxiv.

Identification of holocarboxylase synthetase (HCS) proteins in human placenta.

M. Hiratsuka, Y. Suzuki, K. Narisawa, 1998, Biochimica et biophysica acta.

Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patients.

Kazutoshi Takahashi, Xia Li, R. Sakuta, 1995, Biochimica et biophysica acta.

Molecular analysis of new Japanese patients with holocarboxylase synthetase deficiency

N. Shimizu, M. Hiratsuka, J. Kudoh, 1998, Journal of Inherited Metabolic Disease.

SARS-CoV-2 infection in patients with primary Sjögren syndrome: characterization and outcomes of 51 patients

A. Vissink, F. Giardina, D. Isenberg, 2020, Rheumatology.

Prevalence of primary Sjögren's syndrome in China.

Q. Yao, Yi-huan Dong, Y. Dong, 1995, The Journal of rheumatology.

SAT0683 A north-south worldwide gradient in systemic activity of primary sjÖgren syndrome: increased severe disease in patients from southern countries

D. Isenberg, J. Gottenberg, V. Devauchelle-Pensec, 2018, Saturday, 16 JUNE 2018.