Annotated Bibliography

Research Paper: Annotated Bibliography Assignment Instructions

Overview

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The Research Paper: Annotated Bibliography Assignment is designed to assist you with understanding your research paper references, to teach you how to annotate scholarly journal articles and to give you practice using proper in-text citations. For this assignment, you will be annotating 5 scholarly (peer-reviewed) journal articles.

Instructions

Choose 5 scholarly peer-reviewed journal articles which contain research specific to the disability you have selected for your Research Paper: Final Submission Assignment. Each journal article must have been published in the past 5 years.
Please see Research Paper: Annotated Bibliography Assignment page under the Research Paper: Annotated Bibliography Resources for a link to a sample APA annotation format to check your understanding of the current APA format for annotations in the Liberty Online Library.
Cite the first article in current APA format.
Write a concise annotation (200-250 words) which summarizes the central theme and scope of the article.
Explain why this article might be selected for a summative final research paper (100-150 word). Do not use first person.
Repeat for 4 additional articles.

Current APA style is required.
Each annotation should use current APA Annotation format.
All entries must be scholarly peer reviewed journal articles, published within the past 5 years.
Websites and books are not acceptable sources.
Do not include direct quotes. Instead, paraphrase information from the scholarly sources (using in-text citations) in order to demonstrate your mastery of each concept.
Do not use first person. Write in a formal college-level essay style.

If you need assistance finding scholarly journal articles, please see the Research Paper: Annotated Bibliography Assignment page under the Research Paper: Annotated Bibliography Resources for a link to Liberty’s Online Library.

The Epidemiology, Pathophysiology, Prognosis, and Management of Albinism

References

House, W., & Square, F. (2019). Best Practice: Skin Cancer Prevention and Management for Persons with Albinism in Sub-Saharan Africa, un guide pratique pour la mise en place du programme, la surveillance de la peau et le traitement. Journal officiel de l’International Foundation for Dermatology, (15), 2.

Klatt, E. C., & Kumar, V. (2021). Robbins and Cotran Review of Pathology E-Book. Elsevier Health Sciences.

Kruijt, C. C., de Wit, G. C., Bergen, A. A., Florijn, R. J., Schalij-Delfos, N. E., & van Genderen, M. M. (2018). The phenotypic spectrum of albinism. Ophthalmology, 125(12), 1953-1960.

Marçon, C. R., & Maia, M. (2019). Albinism: epidemiology, genetics, cutaneous characterization, psychosocial factors. Anais brasileiros de dermatologia, 94, 503-520.

Marçon, C. R., Moraes, J. C., de Olivas Ferreira, M. A. M., & Oliari, C. B. (2020). Dermatological and epidemiological profiles of patients with albinism in são paulo, Brazil, between 2010 and 2017: a cross-sectional study. Dermatology, 236(3), 219-227.

Monfermé, S., Lasseaux, E., Duncombe-Poulet, C., Hamel, C., Defoort-Dhellemmes, S., Drumare, I., … & Arveiler, B. (2019). Mild form of oculocutaneous albinism type 1: phenotypic analysis of compound heterozygous patients with the R402Q variant of the TYR gene. British Journal of Ophthalmology, 103(9), 1239-1247.

Moreno‐Artero, E., Morice‐Picard, F., Bremond‐Gignac, D., Drumare‐Bouvet, I., Duncombe‐Poulet, C., Leclerc‐Mercier, S., … & Hadj‐Rabia, S. (2021). Management of albinism: French guidelines for diagnosis and care. Journal of the European Academy of Dermatology and Venereology, 35(7), 1449-1459.

Peralta, R., Sabban, E. C., Friedman, P., Marcucci, C., Garlatti, L. A. B., Galimberti, G., & Cabo, H. (2017). Proposal for management and dermoscopy follow-up of nevi in patients affected by oculocutaneous albinism type Ia. Dermatology practical & conceptual, 7(1), 39.

Sajid, Z., Yousaf, S., Waryah, Y. M., Mughal, T. A., Kausar, T., Shahzad, M., … & Ahmed, Z. M. (2021). Genetic Causes of Oculocutaneous Albinism in Pakistani Population. Genes, 12(4), 492.

Volk, A. E., Hedergott, A., Preising, M., Rading, S., Fricke, J., Herkenrath, P., … & Kubisch, C. (2021). Biallelic mutations in l-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism. Human Genetics, 1-12.

Wu, G., Yan, D., Zhou, M., Li, W., Jiang, P., & Zhu, X. (2020). Neonatal Oculocutaneous Albinism Type 2 With Prader-Willi Syndrome.

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