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Publications by Sarah Low

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

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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)

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A Stop Codon Mutation in SCN9A Causes Lack of Pain Sensation

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Molecular Biology

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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

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Idiopathic Pancreatitis in a Patient With a STAT3 Mutation

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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

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