Suchergebnisse - "Doi, Asako"

PubPharm (131)

41

Was School Closure Effective in Mitigating Coronavirus Disease 2019 (COVID-19)? Time Series Analysis Using Bayesian Inference

enthalten in: Preprints.org | 2020

von Iwata, K. | Doi, A. | Miyakoshi, C.

42

Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young-onset diabetes with exome sequencing

enthalten in: Journal of diabetes investigation | 2020

von Matsutani, N. | Furuta, H. | Matsuno, S. | +9

43

Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant : 6-year clinical course

enthalten in: Journal of diabetes investigation | 2020

von Uraki, S. | Furuta, H. | Miyawaki, M. | +12

44

Comparison between IMP carbapenemase-producing Enterobacteriaceae and non-carbapenemase-producing Enterobacteriaceae : a multicentre prospective study of the clinical and molecular epidemiology of carbapenem-resistant Enterobacteriaceae

enthalten in: The Journal of antimicrobial chemotherapy | 2020

von Hayakawa, K. | Nakano, R. | Hase, R. | +14

45

A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia

enthalten in: Journal of diabetes | 2020

von Karatojima, M. | Furuta, H. | Matsutani, N. | +11

46

Shortening antibiotic duration in the treatment of acute cholangitis : rationale and study protocol for an open-label randomized controlled trial

enthalten in: Trials | 2020

von Iwata, K. | Doi, A. | Oba, Y. | +8

47

Shortening antibiotic duration in the treatment of acute cholangitis: rationale and study protocol for an open-label randomized controlled trial

enthalten in: Trials | 2020

von Iwata, K. | Doi, A. | Oba, Y. | +8

48

Shortening antibiotic duration in the treatment of acute cholangitis: rationale and study protocol for an open-label randomized controlled trial

enthalten in: Trials | 2020

von Iwata, K. | Doi, A. | Oba, Y. | +8

49

A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia

enthalten in: Journal of Diabetes | 2020

von Karatojima, M. | Furuta, H. | Matsutani, N. | +11

50

Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant : 6‐year clinical course

enthalten in: Journal of Diabetes Investigation | 2020

von Uraki, S. | Furuta, H. | Miyawaki, M. | +12