[The gene defect for Finnish hereditary amyloidosis has been found]

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Leukemia·2017

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

Leukemia·2016

MicroRNA-related sequence variations in human cancers.

Human genetics·2013

Recurrent and founder mutations in the PMS2 gene.

Clinical genetics·2012

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

Clinical genetics·2011

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Gut·2010

Update on Current Care Guideline: Psoriasis (skin and joints).

Duodecim; laaketieteellinen aikakauskirja·2017

FOUR score in monitoring the level of consciousness of an intensive care patient: first experience of the use of the Finnish language version.

Duodecim; laaketieteellinen aikakauskirja·2017

Discussing a serious illness with a patient and family.

Duodecim; laaketieteellinen aikakauskirja·2017

Invasive treatment of superficial veins of the lower extremities.

Duodecim; laaketieteellinen aikakauskirja·2017

When should a drain be left in the abdominal cavity upon surgery?

Duodecim; laaketieteellinen aikakauskirja·2017

Diagnostics and current care of myasthenia gravis.

Duodecim; laaketieteellinen aikakauskirja·2017

Mutation-driven structural and functional changes in ACE2 and their potential implications for Alzheimer's disease.

Journal of biomolecular structure & dynamics·2026

Tranilast/roxithromycin with topical tacrolimus in refractory atopic facial eczema: Case report.

International journal of clinical pharmacology and therapeutics·2026

Custom Triflange Acetabular and Femoral Components for Primary Hip Arthroplasty in a Patient With Severe Bone Defect: A Case Report.

Cureus·2026

Open-face plane orientation of a BioMedtrix biologic fixation acetabular cup can be accurately determined from a lateral radiograph.

American journal of veterinary research·2026

Expansion of the Clinical Spectrum of Autosomal Recessive Fatty Acyl-CoA Reductase 1 (FAR1) Deficiency: A Previously Unreported Association With Imperforate Anus-A Case Report.

American journal of medical genetics. Part A·2026

The Pedicled Anterolateral Thigh Flap for Phalloplasty: The Athenian Experience.

Cureus·2026

Related Experiment Videos

[The gene defect for Finnish hereditary amyloidosis has been found]

Related Concept Videos

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

MicroRNA-related sequence variations in human cancers.

Recurrent and founder mutations in the PMS2 gene.

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Update on Current Care Guideline: Psoriasis (skin and joints).

FOUR score in monitoring the level of consciousness of an intensive care patient: first experience of the use of the Finnish language version.

Discussing a serious illness with a patient and family.

Invasive treatment of superficial veins of the lower extremities.

When should a drain be left in the abdominal cavity upon surgery?

Diagnostics and current care of myasthenia gravis.

Mutation-driven structural and functional changes in ACE2 and their potential implications for Alzheimer's disease.

Tranilast/roxithromycin with topical tacrolimus in refractory atopic facial eczema: Case report.

Custom Triflange Acetabular and Femoral Components for Primary Hip Arthroplasty in a Patient With Severe Bone Defect: A Case Report.

Open-face plane orientation of a BioMedtrix biologic fixation acetabular cup can be accurately determined from a lateral radiograph.

Expansion of the Clinical Spectrum of Autosomal Recessive Fatty Acyl-CoA Reductase 1 (FAR1) Deficiency: A Previously Unreported Association With Imperforate Anus-A Case Report.

The Pedicled Anterolateral Thigh Flap for Phalloplasty: The Athenian Experience.

Related Experiment Videos

[The gene defect for Finnish hereditary amyloidosis has been found]

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