Adenosine deaminase deficiency in a child with severe combined immunodeficiency

Health evaluation of volatile organic compound (VOC) emission from exotic wood products.

Indoor air·2009

Rare mtDNA haplogroups and genetic differences in rich and poor Danish Iron-Age villages.

American journal of physical anthropology·2007

Simultaneous detection of ACP1 and GC genotypes using PCR/SSCP.

Annals of human genetics·2003

HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.

Scandinavian journal of clinical and laboratory investigation·2003

Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing result.

Annals of human genetics·2001

Allergologically relevant rubber accelerators in single-use medical gloves.

Contact dermatitis·2000

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

Clinical genetics·2026

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Clinical genetics·2026

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

Clinical genetics·2026

Enhancing Diagnostic Precision in Non-Immune Hydrops Fetalis: The Incremental Value of Whole Exome Sequencing-A Prospective Cohort Study.

Clinical genetics·2026

Rare Novel Genetic Variants of the OFD1 Gene Associated With a Familial Form and a Sporadic Case of Long Bone Atypical Fractures.

Clinical genetics·2026

Glycemic and safety outcomes of the insulin-only bionic pancreas in older adults and individuals with impaired awareness of Hypoglycemia: a post hoc analysis of a randomized pivotal trial.

Diabetes research and clinical practice·2026

Outcomes of patients with Waldenström macroglobulinemia in ICU: a retrospective multicentric study.

Journal of critical care·2026

B Cell Mechanisms Underlie IgG Glycan Alterations in Obesity.

Glycobiology·2026

Mental- and physical-health comorbidity are strongly associated in idiopathic inflammatory myopathies: a multinational cross-sectional e-survey.

Rheumatology international·2026

Inflammatory Rhabdomyoblastic Tumor with Malignant Progression of the Neck: Unique Copy Number Profile Identified by Nanopore Sequencing.

Head and neck pathology·2026

Bridging the Gap Between Chemiluminescence Immunoassay and Liquid Chromatography-Tandem Mass Spectrometry for Infliximab Monitoring: Method Validation and Clinical Comparability Study.

Journal of separation science·2026

Related Experiment Videos

Adenosine deaminase deficiency in a child with severe combined immunodeficiency

Related Concept Videos

Health evaluation of volatile organic compound (VOC) emission from exotic wood products.

Rare mtDNA haplogroups and genetic differences in rich and poor Danish Iron-Age villages.

Simultaneous detection of ACP1 and GC genotypes using PCR/SSCP.

HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.

Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing result.

Allergologically relevant rubber accelerators in single-use medical gloves.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

Enhancing Diagnostic Precision in Non-Immune Hydrops Fetalis: The Incremental Value of Whole Exome Sequencing-A Prospective Cohort Study.

Rare Novel Genetic Variants of the OFD1 Gene Associated With a Familial Form and a Sporadic Case of Long Bone Atypical Fractures.

Glycemic and safety outcomes of the insulin-only bionic pancreas in older adults and individuals with impaired awareness of Hypoglycemia: a post hoc analysis of a randomized pivotal trial.

Outcomes of patients with Waldenström macroglobulinemia in ICU: a retrospective multicentric study.

B Cell Mechanisms Underlie IgG Glycan Alterations in Obesity.

Mental- and physical-health comorbidity are strongly associated in idiopathic inflammatory myopathies: a multinational cross-sectional e-survey.

Inflammatory Rhabdomyoblastic Tumor with Malignant Progression of the Neck: Unique Copy Number Profile Identified by Nanopore Sequencing.

Bridging the Gap Between Chemiluminescence Immunoassay and Liquid Chromatography-Tandem Mass Spectrometry for Infliximab Monitoring: Method Validation and Clinical Comparability Study.

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Adenosine deaminase deficiency in a child with severe combined immunodeficiency

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