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Research article

First published 2017-2

Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2,compared to Sicilian δ β-thalassemia,by BCL11A and SOX6-targeting microRNAs

Thais A Fornari, Carolina Lanaro, Dulcinéia M Albuquerque [...]

Experimental Biology and Medicine

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Research article

First published 2016-4

Original Research: Generation of non-deletional hereditary persistence of fetal hemoglobin β-globin locus yeast artificial chromosome transgenic mouse models: -175 Black HPFH and -195 Brazilian HPFH

Carolina A Braghini, Flavia C Costa, Halyna Fedosyuk [...]

Experimental Biology and Medicine

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Meeting report

First published 1909-5

Persistent Hereditary Œdema Confined to One Leg

H. S. French

Journal of the Royal Society of Medicine

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Other

First published 2010-10

High Alpha-Fetoprotein Persistence after Orchiectomy. On a Case of Uncommon Etiology

Paolo Chierigo, Oliviero Puccetti, Alfonsino Visonà [...]

Urologia Journal

Free access

Meeting report

First published 1917-5

Persistent Hereditary Œdema of the Legs (Milroy's Disease) in Mother and Daughter

J. D. Rolleston

Journal of the Royal Society of Medicine

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Research article

First published 2022-12

Epidemiology and clinical presentation of feline presumed hereditary or breed-related ocular diseases in France: retrospective study of 129 cats

Matthieu MP Bott, Sabine Chahory

Journal of Feline Medicine and Surgery

Free access

Research article

First published 2023-3

Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family

Miniar Kalai, Imen Moumni, Houyem Ouragini [...]

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

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Research article

First published 2007-11

Lymphedema of the Lower Extremity: Is It Genetic or Nongenetic?

Marwan Shinawi

Clinical Pediatrics

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Research article

First published 2023-3

A Case of Refractory Angioedema

Thomas M. Irwin, Thomas M. Irwin, Andrew Longanecker [...]

Journal of Intensive Care Medicine

Open access

Case report

First published 2020-3

IgA nephropathy suspected to be combined with Fabry disease or Alport syndrome: a case report

Wen Hao, Lina Ao, Chenli Zhang [...]

Journal of International Medical Research

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