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Literature DB >> 30076157

European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia: a guideline review.

Abstract

Entities: Disease

Keywords: bronchiectasis; high-speed video microscopy analysis; nasal nitric oxide; primary ciliary dyskinesia; transmission electron microscopy

Year: 2018 PMID： 30076157 DOI： 10.1136/archdischild-2017-312902

Source DB: PubMed Journal: Arch Dis Child Educ Pract Ed ISSN： 1743-0585 Impact factor: 1.309

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Cited

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8 in total

1. Primary Ciliary Dyskinesia (PCD): A genetic disorder of motile cilia.

Authors: Margaret W Leigh; Amjad Horani; BreAnna Kinghorn; Michael G O'Connor; Maimoona A Zariwala; Michael R Knowles
Journal: Transl Sci Rare Dis Date: 2019-07-04

2. Genetic Basis of Human Congenital Heart Disease.

Authors: Shannon N Nees; Wendy K Chung
Journal: Cold Spring Harb Perspect Biol Date: 2020-09-01 Impact factor: 9.708

3. Primary Ciliary Dyskinesia as a Cause of Repeating Atelectasis in the Neonatal Period.

Authors: Arlete Esteves Lopes Primo; Romy Schmidt Brock Zacharias; Amanda Dias de Moraes; Luiz Vicente Ribeiro Ferreira da Silva Filho; Daniela Rodriguez Trujillo; Renata de Araújo Monteiro Yoshida; Arno Noberto Warth; Celso Moura Rebello
Journal: Am J Case Rep Date: 2020-06-11

4. Severe pulmonary disease in an adult primary ciliary dyskinesia population in Brazil.

Authors: Mary Anne Kowal Olm; Fernando Augusto Lima Marson; Rodrigo Abensur Athanazio; Naomi Kondo Nakagawa; Mariangela Macchione; Niki Tomas Loges; Heymut Omran; Samia Zahi Rached; Carmen Sílvia Bertuzzo; Rafael Stelmach; Paulo Hilário Nascimento Saldiva; José Dirceu Ribeiro; Marcus Herbert Jones; Thais Mauad
Journal: Sci Rep Date: 2019-06-18 Impact factor: 4.379

European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia: a guideline review.

1. Primary Ciliary Dyskinesia (PCD): A genetic disorder of motile cilia.

2. Genetic Basis of Human Congenital Heart Disease.

3. Primary Ciliary Dyskinesia as a Cause of Repeating Atelectasis in the Neonatal Period.

4. Severe pulmonary disease in an adult primary ciliary dyskinesia population in Brazil.

5. HY-DIN' in the Cilia: Discovery of Central Pair-related Mutations in Primary Ciliary Dyskinesia.

6. Frequenting Sequencing: How Genetics Teaches Us Cilia Biology.

7. Kartagener syndrome: A case report.

8. Understanding Primary Ciliary Dyskinesia: Experience From a Mediterranean Diagnostic Reference Centre.