[Histopathology and classification of glomerulonephritis]

De novo assembly and annotation of the North American bison (Bison bison) reference genome and subsequent variant identification.

Animal genetics·2021

Mind-Craft: Exploring the Effect of Digital Visual Experience on Changes to Orientation Sensitivity in Visual Contour Perception.

Perception·2020

Determining the IgG concentrations in bovine colostrum and calf sera with a novel enzymatic assay.

Journal of animal science and biotechnology·2018

Identification of Brucella spp. in feral swine (Sus scrofa) at abattoirs in Texas, USA.

Zoonoses and public health·2017

Healthful dietary patterns and long-term weight change among women with a history of gestational diabetes mellitus.

International journal of obesity (2005)·2016

The quest for a true One Health perspective of brucellosis.

Revue scientifique et technique (International Office of Epizootics)·2015

[Interpretation of questionnaires. An translation method problem].

Nordisk medicin·1999

[Assessment of patients' health status--review of the literature and assessment methods].

Nordisk medicin·1999

[Cognitive and affective dysfunction in MS].

Nordisk medicin·1999

[Hospital-based advanced home-care, models from Ekenäs, Finland].

Nordisk medicin·1999

[How much is the workload of surgeons in Scandinavia?].

Nordisk medicin·1999

[Latex allergy].

Nordisk medicin·1999

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Frontiers in genetics·2026

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

Frontiers in pediatrics·2026

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Epilepsia·2026

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Seizure·2026

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[Histopathology and classification of glomerulonephritis]

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De novo assembly and annotation of the North American bison (Bison bison) reference genome and subsequent variant identification.

Mind-Craft: Exploring the Effect of Digital Visual Experience on Changes to Orientation Sensitivity in Visual Contour Perception.

Determining the IgG concentrations in bovine colostrum and calf sera with a novel enzymatic assay.

Identification of Brucella spp. in feral swine (Sus scrofa) at abattoirs in Texas, USA.

Healthful dietary patterns and long-term weight change among women with a history of gestational diabetes mellitus.

The quest for a true One Health perspective of brucellosis.

[Interpretation of questionnaires. An translation method problem].

[Assessment of patients' health status--review of the literature and assessment methods].

[Cognitive and affective dysfunction in MS].

[Hospital-based advanced home-care, models from Ekenäs, Finland].

[How much is the workload of surgeons in Scandinavia?].

[Latex allergy].

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Related Experiment Videos

[Histopathology and classification of glomerulonephritis]

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