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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, 2019-04, 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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An hour-specific transcutaneous bilirubin nomogram for Mongolian neonates

European journal of pediatrics, 2015-10, Vol.174 (10), p.1299-1304

2015

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

Human genome variation, 2018-04, 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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B-1 B Cells Mediate Required Early T Cell Recruitment to Elicit Protein-Induced Delayed-Type Hypersensitivity

The Journal of immunology (1950), 2003-12, Vol.171 (11), p.6225-6235

2003

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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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Early Local Generation of C5a Initiates the Elicitation of Contact Sensitivity by Leading to Early T Cell Recruitment

The Journal of immunology (1950), 2000-08, Vol.165 (3), p.1588-1598

2000

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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

An hour-specific transcutaneous bilirubin nomogram for Mongolian neonates

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

B-1 B Cells Mediate Required Early T Cell Recruitment to Elicit Protein-Induced Delayed-Type Hypersensitivity

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

Early Local Generation of C5a Initiates the Elicitation of Contact Sensitivity by Leading to Early T Cell Recruitment

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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