Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis ; volume:19 ; number:1 ; day:5 ; month:1 ; year:2018 ; pages:1-5 ; date:12.2018
BMC medical genetics ; 19, Heft 1 (5.1.2018), 1-5, 12.2018
- Urheber
-
Fonseca, Paula Fernanda Silva
- Beteiligte Personen und Organisationen
-
Cançado, Rodolfo Delfini
Naoum, Flavio Augusto
Dinardo, Carla Luana
Fonseca, Guilherme Henrique Hencklain
Gualandro, Sandra Fatima Menosi
Krieger, José Eduardo
Pereira, Alexandre Costa
Brissot, Pierre
Santos, Paulo Caleb Junior Lima
SpringerLink (Online service)
- DOI
-
10.1186/s12881-017-0513-5
- URN
-
urn:nbn:de:1111-201803025179
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:46 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Fonseca, Paula Fernanda Silva
- Cançado, Rodolfo Delfini
- Naoum, Flavio Augusto
- Dinardo, Carla Luana
- Fonseca, Guilherme Henrique Hencklain
- Gualandro, Sandra Fatima Menosi
- Krieger, José Eduardo
- Pereira, Alexandre Costa
- Brissot, Pierre
- Santos, Paulo Caleb Junior Lima
- SpringerLink (Online service)
Ähnliche Objekte (12)
Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease
BARD1 deletion in a patient with suspected hereditary colorectal cancer
Pes cavus and hereditary neuropathies: when a relationship should be suspected
Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome
Retrospective phenotypic and gtenotypic data analysis of 683 patients with suspected hereditary fibrinogen deficiency
DAHEAN: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patients
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer
Coronary Artery Z-scores in Febrile Children with Suspected Kawasaki's Disease—The Value of Serial Echocardiography
Genotypic discrepancies arising from imputation
A male with primary accessory breast carcinoma in an axilla is strongly suspected of having hereditary breast cancer
Comparison of VTE risk scores in guidelines for VTE diagnosis in nonsurgical hospitalized patients with suspected VTE
Hereditary nephritis
Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease
BARD1 deletion in a patient with suspected hereditary colorectal cancer
Pes cavus and hereditary neuropathies: when a relationship should be suspected
Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome
Retrospective phenotypic and gtenotypic data analysis of 683 patients with suspected hereditary fibrinogen deficiency
DAHEAN: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patients
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer
Coronary Artery Z-scores in Febrile Children with Suspected Kawasaki's Disease—The Value of Serial Echocardiography
Genotypic discrepancies arising from imputation
A male with primary accessory breast carcinoma in an axilla is strongly suspected of having hereditary breast cancer
Comparison of VTE risk scores in guidelines for VTE diagnosis in nonsurgical hospitalized patients with suspected VTE
Hereditary nephritis
Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease
BARD1 deletion in a patient with suspected hereditary colorectal cancer
Pes cavus and hereditary neuropathies: when a relationship should be suspected
Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome
Retrospective phenotypic and gtenotypic data analysis of 683 patients with suspected hereditary fibrinogen deficiency
DAHEAN: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patients
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer
Coronary Artery Z-scores in Febrile Children with Suspected Kawasaki's Disease—The Value of Serial Echocardiography
Genotypic discrepancies arising from imputation
A male with primary accessory breast carcinoma in an axilla is strongly suspected of having hereditary breast cancer
Comparison of VTE risk scores in guidelines for VTE diagnosis in nonsurgical hospitalized patients with suspected VTE