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Publications by Rainer Fagerholm

Two Missense Mutations in KCNQ1 Cause Pituitary Hormone Deficiency and Maternally Inherited Gingival Fibromatosis

Nature Communications

Molecular Biology

English

Performance of Automated Scoring of ER, PR, HER2, CK5/6 and EGFR in Breast Cancer Tissue Microarrays in the Breast Cancer Association Consortium

The Clinical Journal of Pathology

English

Related publications

Feline Congenital Erythropoietic Porphyria: Two Homozygous UROS Missense Mutations Cause the Enzyme Deficiency and Porphyrin Accumulation

Molecular Medicine

Molecular Medicine

Molecular Biology

English

Non-Acquired Combined Pituitary Hormone Deficiency

English

Multiple Pituitary Hormone Deficiency: Beware of Combined Hormones Deficiency

International Journal of Pediatric Endocrinology

English

Gingival Fibromatosis-Facial Dysmorphism Syndrome

English

Gingival Fibromatosis: Clinical, Molecular and Therapeutic Issues

Orphanet Journal of Rare Diseases

English

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Internal Medicine

English

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Yearbook of Paediatric Endocrinology

English

Functional Characterization of Two Missense Mutations in Pex5p—C11S and N526K

Biochimica et Biophysica Acta - Molecular Cell Research

Molecular Biology

English

Combined Pituitary Hormone Deficiency - Lessons From the Murine Models

European Journal of Endocrinology

English