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Relevant bibliographies by topics / Acanthosis nigricans- AN

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Academic literature on the topic 'Acanthosis nigricans- AN'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Acanthosis nigricans- AN"

1

Callanan, Niamh, and Neil Wright. "Single-centre case–control study investigating the association between acanthosis nigricans, insulin resistance and type 2 diabetes in a young, overweight, UK population." BMJ Paediatrics Open 6, no. 1 (2022): e001574. http://dx.doi.org/10.1136/bmjpo-2022-001574.

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ObjectiveTo determine the extent to which the presence of acanthosis nigricans confers additional risk for insulin resistance, in addition to obesity alone (body mass index, BMI) within a young, overweight, UK population.Research design and methodsRetrospective data were collected to compare the degree of insulin resistance within a sample of 94 young people with acanthosis nigricans, and a matched cohort of 94 participants with obesity alone. Insulin resistance was assessed by fasting glucose, fasting insulin and Homeostatic Model Assessment of insulin resistance (HOMA-IR) score (a mathematic

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Doležel, Zdeněk, Jana Šťastná, Jan Papež, and Petra Konečná. "Acanthosis nigricans." Pediatrie pro praxi 21, no. 1 (2020): 54–55. http://dx.doi.org/10.36290/ped.2020.005.

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Gibson, Lawrence E. "Acanthosis Nigricans." Mayo Clinic Proceedings 79, no. 12 (2004): 1571. http://dx.doi.org/10.4065/79.12.1571.

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Fargnoli, Maria Concetta, and Pasquale Frascione. "Acanthosis Nigricans." New England Journal of Medicine 353, no. 26 (2005): 2797. http://dx.doi.org/10.1056/nejmicm050300.

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Schwartz, Robert A. "Acanthosis nigricans." Journal of the American Academy of Dermatology 31, no. 1 (1994): 1–19. http://dx.doi.org/10.1016/s0190-9622(94)70128-8.

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Vinzio, S., F. Luca, B. Cribier, and J. L. Schlienger. "Acanthosis nigricans." Médecine des Maladies Métaboliques 3, no. 5 (2009): 519. http://dx.doi.org/10.1016/s1957-2557(09)73301-2.

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De Schepper, S., and J. M. Naeyaert. "Acanthosis nigricans." EMC - Dermatologie 1, no. 1 (2006): 1–7. http://dx.doi.org/10.1016/s0246-0319(06)41636-8.

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Matsuoka, Lois Y., Jacobo Wortsman, and Jose Goldman. "Acanthosis nigricans." Clinics in Dermatology 11, no. 1 (1993): 21–25. http://dx.doi.org/10.1016/0738-081x(93)90076-o.

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Sedano, Heddie O., and Robert J. Gorlin. "Acanthosis nigricans." Oral Surgery, Oral Medicine, Oral Pathology 63, no. 4 (1987): 462–67. http://dx.doi.org/10.1016/0030-4220(87)90259-3.

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10

Marimuthu, S., and B. S. Menon. "Acanthosis nigricans." Archives of Disease in Childhood 94, no. 6 (2009): 477. http://dx.doi.org/10.1136/adc.2008.155713.

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Dissertations / Theses on the topic "Acanthosis nigricans- AN"

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FREDEVAL, HELENE. "Acanthosis nigricans." Nantes, 1991. http://www.theses.fr/1991NANT024M.

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Battistelli, Christine. "Acanthosis nigricans bénin familial : étude d'un cas et revue de la littérature." Université Louis Pasteur (Strasbourg) (1971-2008), 1989. http://www.theses.fr/1989STR1M099.

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Eidson, Andrea Christine, and Andrea Christine Eidson. "Acanthosis Nigricans: A Risk Factor for Type II Diabetes." Thesis, The University of Arizona, 2017. http://hdl.handle.net/10150/624974.

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This paper serves as a review of Type II diabetes and pre-diabetes and their associated risk factors: obesity, race, age, and family history of the disease. A new risk factor, Acanthosis Nigricans, is examined in ordinance with common diabetes risk factors, and correlations are drawn between its occurrence and Type II diabetes. Acanthosis Nigricans is a skin condition that can be non-invasively identified. With the current rise of diabetes and obesity in children and adults, finding an easily identifiable risk factor is pertinent for catching the disease in the pre-diabetic state before

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FIMBEL, SYLVIE. "Les troubles endocriniens lies a l'acanthosis nigricans : insulinoresistance et hyperandrogenie ; implications cliniques et physiopathologiques ; a propos de 13 observations." Lyon 1, 1992. http://www.theses.fr/1992LYO1M075.

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Cornille, Maxence. "Etude de la physiopathologie du syndrome de Crouzon avec acanthosis nigricans lié à FGFR3." Thesis, Paris Sciences et Lettres (ComUE), 2019. http://www.theses.fr/2019PSLET051.

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Fibroblast Growth Factor Receptor 3 (Fgfr3) est un récepteur à activité tyrosine kinase. Sa fonction est de réguler la survie, la prolifération et la différenciation cellulaire dans de nombreux tissus.Les mutations gain-de-fonction du gène codant Fgfr3 sont responsables de deux types de maladies génétiques : les chondrodysplasies, caractérisées par des anomalies de la croissance des os longs, et les craniosynostoses, caractérisées par une fusion prématurée des sutures crâniennes. Les patients atteints de craniosynostoses liées à des mutations du gène Fgfr3 présentent également des troubles com

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Battista, Michelle. "School Health Screening and the Utility of Acanthosis Nigricans to Assess for Metabolic Change." The Ohio State University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=osu1291148293.

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Boisvilliers, Fabienne de. "L'insulinorésistance dans le syndrome des ovaires polykystiques avec acanthosis nigricans : étude clinique et biologique de cinq cas." Montpellier 1, 1992. http://www.theses.fr/1992MON11050.

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Arpin-Bott, Marie-Pierre. "Exploration des syndromes d'insulino-resistance extreme avec acanthosis nigricans et hyperandrogenisme : a propos de 2 cas." Université Louis Pasteur (Strasbourg) (1971-2008), 1985. http://www.theses.fr/1985STR1M191.

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Rachidi, Amine. "Acanthosis nigricans de diagnostic étiologique difficile, à propos d'une observation s'accompagnant d'une biologie lupique et révélant un thymome." Bordeaux 2, 1998. http://www.theses.fr/1998BOR2M076.

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Books on the topic "Acanthosis nigricans- AN"

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Parker, James N., and Philip M. Parker. Crouzonodermoskeletal syndrome: A bibliography and dictionary for physicians, patients, and genome researchers [to internet references]. ICON Health Publications, 2007.

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Publications, ICON Health. Acanthosis Nigricans - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References. ICON Health Publications, 2004.

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Archer, Charles M. G., and Clive B. Archer. Skin markers of internal medicine. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0260.

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Some of the most interesting aspects of dermatology are seen when internal medicine and dermatology overlap. Skin lesions may be part of a systemic disease, as occurs in sarcoidosis or SLE, or may be a manifestation or ‘marker’ of an underlying disease or process, as in acanthosis nigricans. Here, we will focus on the diagnosis and treatment of selected skin markers of internal medicine.

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Sybert, Virginia P. Disorders of The Epidermis: Differentiation and Kinetics. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0002.

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Ichthyoses – Bullous Congenital Ichthyosiform Erythroderma – Continual Peeling Skin – Harlequin Fetus – Ichthyosis Bullosa of Siemens – Ichthyosis Hystrix – Ichthyosis Vulgaris – Lamellar Exfoliation of the Newborn – Lamellar Ichthyosis/Nonbullous Congenital Ichthyosiform Erythroderma – Netherton Syndrome – Restrictive Dermopathy – X-linked Recessive Ichthyosis – Erythrokeratodermas – Erythrokeratodermia Variabilis – Pityriasis Rubra Pilaris – Progressive Symmetric Erythrokeratoderma – Acrokeratoderma – Acrokeratoelastoidosis – Acrokeratosis Verruciformis (HOPF) – Hereditary Palmoplantar Kerat

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Sybert, Virginia P. Disorders of the Epidermis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0002.

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Chapter 2 covers Ichthyoses (Bullous Congenital Ichthyosiform Erythroderma, Harlequin Ichthyosis, Ichthyosis Bullosa of Siemens, Ichthyosis Hystrix, Ichthyosis Vulgaris, Lamellar Exfoliation of the Newborn, Lamellar Ichthyosis/Nonbullous Congenital Ichthyosiform Erythroderma, Netherton Syndrome, Peeling Skin Syndrome, Restrictive Dermopathy, and X-linked Recessive Ichthyosis), Erythrokeratodermas (Erythrokeratodermia Variabilis ET PROGESSIVA, and Pityriasis Rubra Pilaris), Acrokeratoderma (Acrokeratoelastoidosis, Acrokeratosis Verruciformis (HOPF)), Hereditary Palmoplantar Keratodermas (Heredi

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Book chapters on the topic "Acanthosis nigricans- AN"

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Ronger Savle, Sandra. "Acanthosis Nigricans." In Vulvar Disease. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-61621-6_39.

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Saleh, Mohamed, and Radhika Muzumdar. "Acanthosis Nigricans." In Endocrine Conditions in Pediatrics. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-52215-5_18.

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Fry, Lionel, Fenella T. Wojnarowska, and Parvin Shahrad. "Acanthosis Nigricans." In Illustrated Encyclopedia of Dermatology. Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-010-9390-3_1.

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Scharnagl, Hubert, Winfried März, Markus Böhm, et al. "Acanthosis Nigricans." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_12.

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Gammanpila, Ranthilaka R., and Eckart Haneke. "Acanthosis Nigricans." In Dermatoses in Dark Vs Light Skin. CRC Press, 2025. https://doi.org/10.1201/9781003479512-1.

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Scharnagl, Hubert, Winfried März, Markus Böhm, et al. "Acanthosis Nigricans Maligna." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_6323.

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Dietrich, Vanessa, Lea Bielicky, Attila Antal, Michael J. Flaig, and Rita Varga. "Acanthosis nigricans bei Urothelkarzinom." In Fortschritte der praktischen Dermatologie und Venerologie 2012. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-24767-5_92.

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Reissig, Federico. "Insulin Resistance and Acanthosis Nigricans." In Dermatology and Diabetes. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-72475-1_8.

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Pustover, Kaylan, Katelynn Campbell, and Michael B. Morgan. "Acquired Ichthyosis, Acanthosis Nigricans, and Palmar Hyperkeratosis." In Deadly Dermatologic Diseases. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31566-9_16.

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Ismail, Aya Badeea, and Mahmut Cerkez Ergoren. "Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans Syndrome." In Genetic Syndromes. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-319-66816-1_1377-1.

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Conference papers on the topic "Acanthosis nigricans- AN"

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DURU, Serap, OZLEM SEVER, MELİKE YÜCEEGE, ATA ALBAYRAK, AYNUR T. ARIKÖK, and SADIK ARDIÇ. "ACANTHOSIS NIGRICANS IN A PATIENT WITH LUNG CANCER: CASE REPORT." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a4720.

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Ice, Christa, Emily Murphy, Lesley Cottrell, William Neal, and Giovanni Piedimonte. "Associations Between Acanthosis Nigricans, Insulin, And Asthma In Rural, Appalachian Children." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a1774.

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Бричева, Э. Б., Л. И. Зильберман та Д. Н. Лаптев. "КЛИНИЧЕСКИЙ СЛУЧАЙ МАНИФЕСТАЦИИ САХАРНОГО ДИАБЕТА 1 ТИПА НА ФОНЕ ОЖИРЕНИЯ У ПОДРОСТКА ПОСЛЕ ПЕРЕНЕСЕННОЙ НОВОЙ КОРОНАВИРУСНОЙ ИНФЕКЦИИ". У X (XXIX) НАЦИОНАЛЬНЫЙ КОНГРЕСС ЭНДОКРИНОЛОГОВ с международным участием «Персонализированная медицина и практическое здравоохранение». ФГБУ «НМИЦ эндокринологии» Минздрава России, 2023. http://dx.doi.org/10.14341/cong23-26.05.23-61.

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Поражения не респираторных органов после перенесенной новой коронавирусной инфекции, как пра- вило, возникают не сразу и поздно диагностируются. Однако, нельзя забывать, что COVID-19, как и другие вирусные инфекции, является фактором риска развития сахарного диабета 1 типа (СД1). ЦЕЛЬ: своевременная диагностика СД1 после перенесенной коронавирусной инфекции. КЛИНИЧЕСКИЙ СЛУЧАЙ: мальчик И., в октябре 2021, в возрасте 13 лет обратился в ГНЦ ФГБУ «НМИЦ Эндокринологии» с жалобами на резкую потерю в весе, повышенную жажду, учащенное мочеиспускание. Из анамнеза из

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Кураева, Т. Л., Ю. А. Сергеева, И. А. Еремина, С. В. Попов, Д. Н. Лаптев та В. А. Петеркова. "СЕМЕЙНЫЙ СЛУЧАЙ CАХАРНОГО ДИАБЕТА 2 ТИПА У ПОДРОСТКА С ГЕТЕРОЗИГОТНОЙ МУТАЦИЕЙ В ГЕНЕ AKT2". У X (XXIX) НАЦИОНАЛЬНЫЙ КОНГРЕСС ЭНДОКРИНОЛОГОВ с международным участием «Персонализированная медицина и практическое здравоохранение». ФГБУ «НМИЦ эндокринологии» Минздрава России, 2023. http://dx.doi.org/10.14341/cong23-26.05.23-75.

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Молекулярно-генетические исследования у подростков с сахарным диабетом 2 типа (СД2) привлекает особое внимание в силу слабой изученности и большого вклада генетических факторов в процессы ран- него развития СД2, ранее считавшегося заболеванием пожилого возраста. ЦЕЛЬ: описание результатов исследования семейного случая СД2 у подростка с выраженным ожире- нием и инсулинорезистентностью. Клинический случай: пациент А, 16 лет, наблюдается в дет. отделении ГНЦ ФГБУ «НМИЦ Эндокринологии» МЗ РФ в теч. 2 лет. Из анамнеза: масса тела при рождении 3200 гр., рост 51 см

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