UB Paderborn / Katalog / Suche / in CDI

1 – 9 von 9

Sortiert nach

Iranian hereditary hemochromatosis patients: baseline characteristics, laboratory data and gene mutations

Medical science monitor, 2012-10, Vol.18 (10), p.CR622-CR629

2012

Link zum Volltext

Verfügbarkeit prüfen

Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect

Orphanet journal of rare diseases, 2020-01, Vol.15 (1), p.14-14, Article 14

2020

Link zum Volltext

Verfügbarkeit prüfen

Egg consumption and risk of cardiovascular disease: a PERSIAN cohort-based study

BMC cardiovascular disorders, 2023-11, Vol.23 (1), p.588-588, Article 588

2023

Link zum Volltext

Verfügbarkeit prüfen

Muscle thickness and pennation angle in overweight persons with moderate haemophilia A after resistance and combined training: A randomized controlled trial

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-05, Vol.28 (3), p.505-514

2022

Link zum Volltext

Verfügbarkeit prüfen

Health related quality of life of Iranian children with type 1 diabetes: reliability and validity of the Persian version of the PedsQL™ Generic Core Scales and Diabetes Module

Health and quality of life outcomes, 2011-11, Vol.9 (1), p.104-104, Article 104

2011

Link zum Volltext

Verfügbarkeit prüfen

Confronting infertility in Iranian clients: a grounded theory

Human fertility (Cambridge, England), 2017-10, Vol.20 (4), p.236-247

2017

Link zum Volltext

Verfügbarkeit prüfen

Types and outcomes of cytopenia in critically ill patients

Journal of comparative effectiveness research, 2020-06, Vol.9 (9), p.627-637

2020

Link zum Volltext

Verfügbarkeit prüfen

The effect of an education-based intervention on self-reported awareness and practice of Iranian nurses in observing patients' rights

Global journal of health science, 2014-11, Vol.7 (3), p.98-104

2014

Link zum Volltext

Verfügbarkeit prüfen

A rare form of limb girdle muscular dystrophy (type 2E) seen in an Iranian family detected by autozygosity mapping

Journal of neurogenetics, 2016-01, Vol.30 (1), p.1-4

2016

Link zum Volltext

Verfügbarkeit prüfen

1 – 9 von 9

Suche als RSS-Feed

Aktive Filter

ThemaAdult

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(8)
Mit Volltextzugriff
(8)

Publikationsform

Artikel
(9)

Sprache

Englisch
(9)

Erscheinungsjahr

n.n

Thema

Humans
(9)
Life Sciences & Biomedicine
(8)
Science & Technology
(8)
Female
(6)
Iran
(6)
Male
(6)
Child
(3)
Disease
(3)
Adolescent
(2)
Autozygosity Mapping
(2)
Diabetes
(2)
Genetics & Heredity
(2)
Health Aspects
(2)
Health Care Sciences & Services
(2)
Iran - Epidemiology
(2)
Medicine, Research & Experimental
(2)
Middle Aged
(2)
Muscular Dystrophies, Limb-Girdle - Genetics
(2)
Mutation - Genetics
(2)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Iranian hereditary hemochromatosis patients: baseline characteristics, laboratory data and gene mutations

Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect

Egg consumption and risk of cardiovascular disease: a PERSIAN cohort-based study

Muscle thickness and pennation angle in overweight persons with moderate haemophilia A after resistance and combined training: A randomized controlled trial

Health related quality of life of Iranian children with type 1 diabetes: reliability and validity of the Persian version of the PedsQL™ Generic Core Scales and Diabetes Module

Confronting infertility in Iranian clients: a grounded theory

Types and outcomes of cytopenia in critically ill patients

The effect of an education-based intervention on self-reported awareness and practice of Iranian nurses in observing patients' rights

A rare form of limb girdle muscular dystrophy (type 2E) seen in an Iranian family detected by autozygosity mapping

Aktive Filter

Suchergebnisse filtern