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Publications by Wendye Robbins

Complex Management of a Patient With Refractory Primary Erythromelalgia Lacking a SCN9A Mutation

Journal of Pain Research

English

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Primary Erythromelalgia: A Review

Orphanet Journal of Rare Diseases

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Uncommon Spreading of Primary Malignant Paraganglioma in a Patient With SDHB Mutation

Case Reports in Internal Medicine

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Primary (Genetically Determined) Dilation Cardiomyopathy in a Patient With Novel Mutation of Lamin Gene: Clinical and Morphological Management

Cardiovascular Therapy and Prevention (Russian Federation)

Cardiovascular Medicine

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A Stop Codon Mutation in SCN9A Causes Lack of Pain Sensation

Human Molecular Genetics

Molecular Biology

English

Review of Primary and Secondary Erythromelalgia

Clinical and Experimental Dermatology

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An Acquired NRAS Mutation Contributes to Neutrophilic Progression in a Patient With Primary Myelofibrosis

British Journal of Haematology

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Laparoscopic Management of Primary Ovarian Leimyoma in a Patient With Pelvic Kidney : A Case Report

Gynecology Obstetrics & Reproductive Medicine

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Idiopathic Pancreatitis in a Patient With a STAT3 Mutation

Allergy & Rhinology

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Identification of a Novel Mutation of the PRKAR1A Gene in a Patient With Carney Complex With Significant Osteoporosis and Recurrent Fractures

English