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Novel SYNGAP1 variant in a patient with intellectual disability and distinctive dysmorphisms

Congenital anomalies, 2018-11, Vol.58 (6), p.188-190

2018

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Refining the clinical phenotype of Okur-Chung neurodevelopmental syndrome

Human genome variation, 2018-03, Vol.5 (1), p.18011-18011, Article 18011

2018

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Novel COL2A1 variants in Japanese patients with spondyloepiphyseal dysplasia congenita

Human genome variation, 2022-05, Vol.9 (1), p.16-16, Article 16

2022

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Discordant phenotype caused by CASK mutation in siblings with NF1

Human genome variation, 2019, Vol.6 (1), p.20-20, Article 20

2019

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Maternal socio-demographic and psychological predictors for risk of developmental delays among young children in Mongolia

BMC pediatrics, 2018-02, Vol.18 (1), p.68-68, Article 68

2018

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Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly

Human genome variation, 2018-01, Vol.5 (1), p.4, Article 4

2018

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Fracture of a Broviac catheter in a low-birth-weight infant

Hong Kong medical journal = Xianggang yi xue za zhi, 2008-10, Vol.14 (5), p.411-413

2008

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Republication: Two Premature Neonates of Congenital Syphilis with Severe Clinical Manifestations

Tropical Medicine and Health, 2015, Vol.43(3), pp.165-170

2015

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A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger

SpringerPlus, 2013-09, Vol.2 (1), p.434-434, Article 434

2013

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Early delayed‐type hypersensitivity eosinophil infiltrates depend on T helper 2 cytokines and interferon‐γ via CXCR3 chemokines

Immunology, 2004-03, Vol.111 (3), p.306-317

2004

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B cell-dependent T cell responses: IgM antibodies are required to elicit contact sensitivity

The Journal of experimental medicine, 2002-11, Vol.196 (10), p.1277-1290

2002

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Cutaneous Immunization Rapidly Activates Liver Invariant Vα14 NKT Cells Stimulating B-1 B Cells to Initiate T Cell Recruitment for Elicitation of Contact Sensitivity

The Journal of experimental medicine, 2003-12, Vol.198 (12), p.1785-1796

2003

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Validation of a transcutaneous bilirubin meter in Mongolian neonates: comparison with total serum bilirubin

BMC pediatrics, 2013-09, Vol.13 (1), p.151-151, Article 151

2013

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Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

Cold Spring Harbor molecular case studies, 2021-06, Vol.7 (3), p.a005991

2021

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Early delayed-type hypersensitivity eosinophil infiltrates depend on T helper 2 cytokines and interferon-(gamma) via CXCR3 chemokines

Immunology, 2004-03, Vol.111 (3), p.306

2004

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Cutaneous immunization rapidly activates liver invariant Valpha14 NKT cells stimulating B-1 B cells to initiate T cell recruitment for elicitation of contact sensitivity

The Journal of experimental medicine, 2003-12, Vol.198 (12), p.1785-1796

2003

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Interleukin-4 deficient (IL-4/-) and STAT-6-/-mice have defective contact sensitivity (CS)

Journal of allergy and clinical immunology, 2002, Vol.109 (1), p.S322-S322

2002

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B Cell–dependent T Cell Responses

The Journal of experimental medicine, 2002-11, Vol.196 (10), p.1277-1290

2002

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Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly

Human genome variation, 2018, Vol.5, p.4-4

2018

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A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger

SpringerPlus, 2013, Vol.2, p.434-434

2013

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Novel SYNGAP1 variant in a patient with intellectual disability and distinctive dysmorphisms

Refining the clinical phenotype of Okur-Chung neurodevelopmental syndrome

Novel COL2A1 variants in Japanese patients with spondyloepiphyseal dysplasia congenita

Discordant phenotype caused by CASK mutation in siblings with NF1

Maternal socio-demographic and psychological predictors for risk of developmental delays among young children in Mongolia

Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly

Fracture of a Broviac catheter in a low-birth-weight infant

Republication: Two Premature Neonates of Congenital Syphilis with Severe Clinical Manifestations

A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger

Early delayed‐type hypersensitivity eosinophil infiltrates depend on T helper 2 cytokines and interferon‐γ via CXCR3 chemokines

B cell-dependent T cell responses: IgM antibodies are required to elicit contact sensitivity

Cutaneous Immunization Rapidly Activates Liver Invariant Vα14 NKT Cells Stimulating B-1 B Cells to Initiate T Cell Recruitment for Elicitation of Contact Sensitivity

Validation of a transcutaneous bilirubin meter in Mongolian neonates: comparison with total serum bilirubin

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

Early delayed-type hypersensitivity eosinophil infiltrates depend on T helper 2 cytokines and interferon-(gamma) via CXCR3 chemokines

Cutaneous immunization rapidly activates liver invariant Valpha14 NKT cells stimulating B-1 B cells to initiate T cell recruitment for elicitation of contact sensitivity

Interleukin-4 deficient (IL-4/-) and STAT-6-/-mice have defective contact sensitivity (CS)

B Cell–dependent T Cell Responses

Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly

A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger

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