一个哲学家的观点.

Laboratory study on leachability of five herbicides in South Australian soils.

Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes·2000

Seeing the wood for the trees: defining the forgotten concept of patient dissatisfaction in the light of patient satisfaction research.

International journal of health care quality assurance incorporating Leadership in health services·2000

GABAA receptor mediated elevation of Ca2+ and modulation of gonadotrophin-releasing hormone action in alphaT3-1 gonadotropes.

Journal of neuroendocrinology·2000

Influence of hypertension, left ventricular hypertrophy, and left ventricular systolic dysfunction on plasma N terminal proBNP.

Heart (British Cardiac Society)·2000

Detection of immunoglobulin antibodies in the sera of patients using purified latex allergens.

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology·2000

Conflicts regarding decisions to limit treatment: a differential diagnosis.

JAMA·2000

Universal gates from braiding and fusing anyons on quantum hardware.

Nature·2026

People use fast and flat simulation to reason about new games.

Nature·2026

Rising dust pollution across Europe in a changing climate.

Nature·2026

Ammonia pressure controls colloidal metal nitride synthesis in molten salts.

Nature·2026

Programming fracture resistance in metamaterials via elastic instabilities.

Nature·2026

Selectivity Emerges from Indiscriminate Photoreduction.

Nature·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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一个哲学家的观点

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Laboratory study on leachability of five herbicides in South Australian soils.

Seeing the wood for the trees: defining the forgotten concept of patient dissatisfaction in the light of patient satisfaction research.

GABAA receptor mediated elevation of Ca2+ and modulation of gonadotrophin-releasing hormone action in alphaT3-1 gonadotropes.

Influence of hypertension, left ventricular hypertrophy, and left ventricular systolic dysfunction on plasma N terminal proBNP.

Detection of immunoglobulin antibodies in the sera of patients using purified latex allergens.

Conflicts regarding decisions to limit treatment: a differential diagnosis.

Universal gates from braiding and fusing anyons on quantum hardware.

People use fast and flat simulation to reason about new games.

Rising dust pollution across Europe in a changing climate.

Ammonia pressure controls colloidal metal nitride synthesis in molten salts.

Programming fracture resistance in metamaterials via elastic instabilities.

Selectivity Emerges from Indiscriminate Photoreduction.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

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一个哲学家的观点

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