Albinism in the Ancient Mediterranean World by John L. Hilton

Subjects: “…Ancient Mediterranean, albinism, the sacred, conception, sacrifice, astral cults…”
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Sociodemographic and visual characteristics of individuals with oculocutaneous albinism in Botswana by Thanuja Panicker, Gopinath Madheswaran

Subjects: “…oculocutaneous albinism…”
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Baudez Claude-François, Une histoire de la religion des Mayas, Albin Michel, coll. « Bibliothèque Albin Michel Histoire », Paris, 2002, 472 p. by Miguel Rivera Dorado

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Reading Pedagogy in EFL Classes for Students with albinism: A case study by Dossou Flavien LANMANTCHION

“…Abstract: Benin Republic encounters socio economic challenges that impact access to education for all children, particularly, those with disabilities like albinism. This paper looked into the practices of teachers in reading and perceptions of students with albinism in English language classes in the Republic of Benin. …”
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A Histopathological Study of Skin Lesions in Individuals with Oculocutaneous Albinism in Togo in 2019 by Bayaki Saka, Julienne Noude Teclessou, Sefako Abla Akakpo, Piham Gnossike, Kwamé Doh, Saliou Adam, Abas Mouhari-Toure, Garba Mahamadou, Panawé Kassang, Yvette Elegbede Moise, Tchin Darre, Koussake Kombate, Palokinam Pitché

“…The aim of this study was to study the histopathological patterns of skin lesions in persons with albinism (PWA) in Togo in 2019. Method. During two mobile skin care clinics in 2019, biopsies/excisional biopsies were performed in PWA in case of clinical doubt or in front of lesions suspected to be cancerous for histological examination. …”
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Albinism of Aesculapian snake Zamenis longissimus (Laurenti, 1768) in situ: first record for Bosnia and Herzegovina by Ana Ćurić

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Richard Sennett, Bâtir et habiter pour une éthique de la ville, Albin Michel, 2019 by Yankel Fijalkow

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First record of albino Aesculapian Snake (Elaphe longissima) in Slovenia by Miha Krofel

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Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome) by Majid Alfadhel, Bashayr S. Alhubayshi, Muhammad Umair, Ahmed Alfaidi, Deemah Alwadaani, Essra Aloyouni, Safdar Abbas, Abdulkareem Al Abdulrahman, Mohammed Aldrees, Abeer Al Tuwaijri, Ruaa S. Alharithy, Abdulaziz Alajlan, Abdulrahman Alswaid, Saad Almohrij, Sultan Al-Khenaizan

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Elena Lasida, 2011, Le goût de l'autre. La crise, une chance pour réinventer le lien, Paris : Albin Michel, 326 p. by Igor Martinache

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Neoklasik Realizm ve Küçük Devlet Yaklaşımı Çerçevesinde Kosova Dış Politikası’nın Değerlendirilmesi by Göktürk TÜYSÜZOĞLU

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Novel Heterogenous CHS1 Mutations Identified in Five Japanese Patients with Chediak-Higashi Syndrome by Fuminori Tanabe, Hirotake Kasai, Michiko Morimoto, Shigeharu Oh, Hidetoshi Takada, Toshiro Hara, Masahiko Ito

“…Chediak-Higashi syndrome (CHS) is a rare, autosomal recessive disorder characterized by oculocutaneous albinism, recurrent bacterial infections and progressive neurological dysfunction. …”
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Eyelash Trichomegaly: Unusual Feature Associated with Systemic Lupus Erythematosus Patient by Amjad M. AlWarawreh, Ahmad M. AlWarawreh, Bashar F. Jarrar, Asem H. Aldebei, Mahasen S. Ajarmeh, Fadi F. Ayyash, Manal A. Abu Al-Ghanam

“…It may occur due to many causes, such as the presence of other disorders such as HIV infection, congenital anomalies like oculocutaneous albinism, or Oliver–McFarlane syndrome. It may be linked to the use of certain drugs and can also be present as an isolated trait by birth. …”
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Late Endocrine Effects after Stem Cell Transplant in a Young Girl with Griscelli Syndrome by Shana R. Mencher, William V. Tamborlane, Anisha D. Patel

“…Griscelli syndrome (GS) is a rare disorder characterized by partial albinism and silver hair with alteration in genes necessary for melanin transport. …”
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Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome by Kasumi Shimizu, Miho Hayashi, Nozomi Ito, Kokoro Hamada, Gaku Koizumi, Kazuto Kurohara, Naoya Arai

“…Chédiak–Higashi syndrome (CHS), a rare autosomal recessive disorder associated with leukocyte dysfunction, is characterised by partial skin and hair albinism, immunodeficiency, and abnormal bleeding. …”
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Investigating the Causes of Blindness and Vision Impairment in Children Younger Than 15 Years Old by Abbas Riazi, Fatemeh Riazi

“…Retinitis pigmentosa 9%, Leber congenital amaurosis (LCA) 8%, albinism <1%, refractive errors 9.5%, cortical visual impairment 13.6%, cataract and glaucoma each alone 7%, corneal opacity 1.7% and non-pathogenic causes, such as trauma <1% were diagnosed. …”
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Molecular-genetic bases of plumage coloring in chicken by A. V. Makarova, O. V. Mitrofanova, A. B. Vakhrameev, N. V. Dementeva

“…The biosynthesis and types of melanin are affected by the activity of the enzyme tyrosine, and mutations in the tyrosinase gene (TYR) cause albinism in different species. The formation mechanism of brown, silver, gold, lavender and a number of other shades is determined by the influence on the work of the MC1R genes and TYR specific modifier genes. …”
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Creation of body color mutants by CRISPR/Cas9 gene editing in largemouth bass, Micropterus salmoides by Lina Sun, Tian Gao, Zhiqiang Li, Xiaolong Yang, Zuliang Qin, Mingxiao Ye, Ying Li, Feilong Wang, Deshou Wang

“…The tyrb mutation resulted in reduced melanin and even albinism in eye and body of larvae, while the csf1ra mutation led to reddish body color, reduced xanthophores and melanophores in juvenile and adult fish with high mutation rate. …”
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