These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 29977761)

  • 1. Alpha1 antitrypsin deficiency due to an homozygous PI* Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expression.
    Jouhadi Z; Odou MF; Zerimech F; Bousfiha AA; Mikou N; Porchet N; Crepin M; Najib J; Balduyck M
    Respir Med Case Rep; 2018; 24():58-62. PubMed ID: 29977761
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a novel alpha1-antitrypsin null variant (Q0Cairo).
    Zorzetto M; Ferrarotti I; Campo I; Balestrino A; Nava S; Gorrini M; Scabini R; Mazzola P; Luisetti M
    Diagn Mol Pathol; 2005 Jun; 14(2):121-4. PubMed ID: 15905697
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Alpha-1 antitrypsin deficiency caused by Null mutation].
    Perrin J; Aimone-Gastin I; Balduyck M; Mercy M; Filhine-Trésarrieu P; Odou MF; Chaouat A; Chabot F
    Rev Mal Respir; 2016 Sep; 33(7):612-7. PubMed ID: 26604020
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical manifestations of a new alpha-1 antitrypsin genetic variant:
    Aiello M; Frizzelli A; Marchi L; Ferrarotti I; Piloni D; Pelà G; De Simoni A; D'Aloisio L; Calzetta L; Chetta A
    Respirol Case Rep; 2022 May; 10(5):e0936. PubMed ID: 35433011
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Alpha-1-antitrypsin (SERPINA1) mutation spectrum: Three novel variants and haplotype characterization of rare deficiency alleles identified in Portugal.
    Silva D; Oliveira MJ; Guimarães M; Lima R; Gomes S; Seixas S
    Respir Med; 2016 Jul; 116():8-18. PubMed ID: 27296815
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alpha-1 antitrypsin Null mutations and severity of emphysema.
    Fregonese L; Stolk J; Frants RR; Veldhuisen B
    Respir Med; 2008 Jun; 102(6):876-84. PubMed ID: 18353624
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a novel SERPINA-1 mutation causing alpha-1 antitrypsin deficiency in a patient with severe bronchiectasis and pulmonary embolism.
    Milger K; Holdt LM; Teupser D; Huber RM; Behr J; Kneidinger N
    Int J Chron Obstruct Pulmon Dis; 2015; 10():891-7. PubMed ID: 26005342
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis.
    Carpagnano GE; Santacroce R; Palmiotti GA; Leccese A; Giuffreda E; Margaglione M; Foschino Barbaro MP; Aliberti S; Lacedonia D
    Lung; 2017 Oct; 195(5):679-682. PubMed ID: 28668972
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Distribution of Alpha-1 Antitrypsin Genotypes Between Patients with COPD/Emphysema, Asthma and Bronchiectasis.
    Veith M; Tüffers J; Peychev E; Klemmer A; Kotke V; Janciauskiene S; Wilhelm S; Bals R; Koczulla AR; Vogelmeier CF; Greulich T
    Int J Chron Obstruct Pulmon Dis; 2020; 15():2827-2836. PubMed ID: 33192056
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Effects of Rare
    Ortega VE; Li X; O'Neal WK; Lackey L; Ampleford E; Hawkins GA; Grayeski PJ; Laederach A; Barjaktarevic I; Barr RG; Cooper C; Couper D; Han MK; Kanner RE; Kleerup EC; Martinez FJ; Paine R; Peters SP; Pirozzi C; Rennard SI; Woodruff PG; Hoffman EA; Meyers DA; Bleecker ER;
    Am J Respir Crit Care Med; 2020 Mar; 201(5):540-554. PubMed ID: 31661293
    [No Abstract]   [Full Text] [Related]  

  • 11. Diagnosis of alpha-1 antitrypsin deficiency: modalities, indications and diagnosis strategy.
    Balduyck M; Odou MF; Zerimech F; Porchet N; Lafitte JJ; Maitre B
    Rev Mal Respir; 2014 Oct; 31(8):729-45. PubMed ID: 25391508
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel alpha1-antitrypsin null variant (PiQ0Milano ).
    Rametta R; Nebbia G; Dongiovanni P; Farallo M; Fargion S; Valenti L
    World J Hepatol; 2013 Aug; 5(8):458-61. PubMed ID: 24023986
    [TBL] [Abstract][Full Text] [Related]  

  • 13. α-1 Antitrypsin Genotype-Phenotype Discrepancy in a 42-Year-Old Man Who Carries the Null-Allele.
    Pavičić T; Ćelap I; Njegovan M; Tešija Kuna A; Štefanović M
    Lab Med; 2020 May; 51(3):301-305. PubMed ID: 31583408
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long-term clinical outcomes following treatment with alpha 1-proteinase inhibitor for COPD associated with alpha-1 antitrypsin deficiency: a look at the evidence.
    Rahaghi FF; Miravitlles M
    Respir Res; 2017 May; 18(1):105. PubMed ID: 28558837
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Case report of a novel alpha1-antitrypsin null variant in Türkiye: Q0
    Karadoğan D; Şahin Ü; Dreger B; Grandoso L; Osaba L
    BMC Pulm Med; 2024 Feb; 24(1):91. PubMed ID: 38383302
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe alpha-1 antitrypsin deficiency in composite heterozygotes inheriting a new splicing mutation QOMadrid.
    Lara B; Martínez MT; Blanco I; Hernández-Moro C; Velasco EA; Ferrarotti I; Rodriguez-Frias F; Perez L; Vazquez I; Alonso J; Posada M; Martínez-Delgado B
    Respir Res; 2014 Oct; 15(1):125. PubMed ID: 25287719
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequency of Rare Alpha-1 Antitrypsin Variants in Polish Patients with Chronic Respiratory Disorders.
    Duk K; Zdral A; Szumna B; Roży A; Chorostowska-Wynimko J
    Adv Exp Med Biol; 2016; 910():47-53. PubMed ID: 26987331
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Panniculitis revealing alpha-1 antitrypsin deficiency. Report of 3 cases].
    Albes B; Bayle-Lebey P; Bazex J; Lamant L
    Ann Med Interne (Paris); 2001 Dec; 152(8):502-6. PubMed ID: 11937984
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Absence of alpha-1-antitrypsin (Pi Null Bellingham) and the early onset of emphysema.
    Cook L; Janus ED; Brenton S; Tai E; Burdon J
    Aust N Z J Med; 1994 Jun; 24(3):263-9. PubMed ID: 7980208
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An Alpha-1 Antitrypsin Deficiency Screening Study in Patients with Chronic Obstructive Pulmonary Disease, Bronchiectasis, or Asthma in Turkey.
    Tural Onur S; Natoli A; Dreger B; Arınç S; Sarıoğlu N; Çörtük M; Karadoğan D; Şenyiğit A; Yıldız BP; Köktürk N; Argun Barıs S; Kodalak Cengiz S; Polatli M
    Int J Chron Obstruct Pulmon Dis; 2023; 18():2785-2794. PubMed ID: 38046982
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.