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Relevant bibliographies by topics / Bisalbuminemie hereditaire

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Academic literature on the topic 'Bisalbuminemie hereditaire'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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Journal articles on the topic "Bisalbuminemie hereditaire"

1

Garcez, Carla, and Susana Carvalho. "Bisalbuminémia: Uma Variante Rara da Albumina." Acta Médica Portuguesa 30, no. 4 (2017): 330. http://dx.doi.org/10.20344/amp.7187.

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Introduction: Bisalbuminemia is a qualitative disorder of albumin and it is defined by the coexistence in the same individual of two types of serum albumin with different electrophoretic mobility. There are two forms: hereditary and permanent, or acquired and transient.Case Report: Girl, 17-years-old, referenced to the hospital consult after incidental finding of bisalbuminemia detected in plasma protein electrophoresis performed within the investigation of diminished muscular tone in the lower limbs. Physical examination was normal. Secondary causes of bisalbuminemia were excluded. Later, it

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Chakravarthy, Srinivas N., and Mathivanan Durairaj. "Bisalbuminemia in an African Male with Sickle Cell Disease." Indian journal of Medical Biochemistry 21, no. 1 (2017): 69–71. http://dx.doi.org/10.5005/jp-journals-10054-0023.

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ABSTRACT Bisalbuminemia is a rare condition characterized by abnormal electrophoretic pattern of serum albumin. There are two types of bisalbuminemia – hereditary and acquired. The acquired type has been reported in chronic renal diseases, pancreatitis, and in patients using beta-lactam antibiotics. The aim of this case report is to discuss the clinical significance of bisalbuminemia in a 58-year-old African male with sickle cell anemia. How to cite this article Chakravarthy SN, Ramanathan S, Menon S, Durairaj M. Bisalbuminemia in an African Male with Sickle Cell Disease. Indian J Med Biochem

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3

Bellomo, A., M. Mancinella, G. Troisi, and V. Marigliano. "A rare familiar case of hereditary bisalbuminemia and diabetic predisposition: A possible predictive link?" Archives of Gerontology and Geriatrics 50, no. 3 (2010): 345–46. http://dx.doi.org/10.1016/j.archger.2009.05.016.

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4

Ugurlu, Serdal, Bugra Han Egeli, and Ibrahim Murat Bolayirli. "Hereditary Bisalbuminemia in Sjögren’s Syndrome and Rheumatoid Arthritis." JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2021. http://dx.doi.org/10.7860/jcdr/2021/46650.14832.

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Bisalbuminemia is rare finding of bifid albumin bands in serum electrophoresis. The protein abnormality can be sporadic and inherited. So far, this albumin variant was not found to cause or coexist with a specific pathology. This is a case of bisalbuminemia in 43-year-old female patient with a past medical history of Rheumatoid Arthritis (RA) and Sjogren’s Syndrome (SS). Similar electrophoresis findings were seen in two siblings of the patient. Rheumatology focused work-up of the family was negative. We could not find an association between this blood protein variant and the patient’s rheumato

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Gili, Claudia, Federico Bonsembiante, Renzo Bonanni, et al. "Detection of hereditary bisalbuminemia in bottlenose dolphins (Tursiops truncatus, Montagu 1821): comparison between capillary zone and agarose gel electrophoresis." BMC Veterinary Research 12, no. 1 (2016). http://dx.doi.org/10.1186/s12917-016-0801-x.

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Dissertations / Theses on the topic "Bisalbuminemie hereditaire"

1

Choplin, Sophie. "Albumine : biosynthèse et anomalies, analbuminénie et bisalbuminémie." Paris 5, 1988. http://www.theses.fr/1988PA05P118.

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