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Do patients with sickle-cell anaemia (HbSS) experience more oral and maxillofacial pain and altered facial sensation than patients with haemoglobin SC (HbSC) disease

Year: 2011

Type: article

Source: International Journal of Oral and Maxillofacial Surgery

DOI: 10.1016/j.ijom.2011.07.654

Authors: M.F. Kiernan, H. Ho, L. Cheng, T. Sato, Q. Naqvi, Z. Imran, R. Amos

Institutions: Homerton University Hospital, Homerton University Hospital NHS Foundation Trust

Language: English

Topic: Hemoglobinopathies and Related Disorders

Subfield: Genetics (clinical)

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Eesti Teadusfondi

OpenAlex ID: W2014530783

FWCI:

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