Robert Fritsche‐Polanz

Mutation analysis of <i>C‐KIT</i> in patients with myelodysplastic syndromes without mastocytosis and cases of systemic mastocytosis

Robert Fritsche‐Polanz, John‐Hendrik Jordan, Alexandra Feix et al. · British Journal of Haematology · 2001 · 141 citations

Indolent Systemic Mastocytosis with Elevated Serum Tryptase, Absence of Skin Lesions, and Recurrent Severe Anaphylactoid Episodes

Stefan Florian, Maria‐Theresa Krauth, Ingrid Simonitsch‐Klupp et al. · International Archives of Allergy and Immunology · 2005 · 79 citations

A Rapid, Highly Sensitive and Open-Access SARS-CoV-2 Detection Assay for Laboratory and Home Testing

Max J. Kellner, James J. Ross, Jakob Schnabl et al. · Frontiers in Molecular Biosciences · 2022 · 57 citations · Full text

Home Testing, Viral Diagnostics, Molecular Biology +20

High frequency of concomitant mastocytosis in patients with acute myeloid leukemia exhibiting the transforming <i>KIT</i> mutation D816V

Robert Fritsche‐Polanz, Marika Fritz, Andrea Huber et al. · Molecular Oncology · 2010 · 48 citations · Full text

Increased prevalence of combined MTR and MTHFR genotypes among individuals with severely elevated total homocysteine plasma levels

Alexandra Feix, Robert Fritsche‐Polanz, Josef Kletzmayr et al. · American Journal of Kidney Diseases · 2001 · 46 citations

Metabolic Syndrome, Combined Mtr, Mthfr Genotypes +8