UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics

Rheumatology (Oxford, England), 2009-08, Vol.48 (8), p.987-991

2009

Volltextzugriff (PDF)

Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children

Rheumatology international, 2012-10, Vol.32 (10), p.3253-3260

2012

Volltextzugriff (PDF)

Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population

European journal of pediatrics, 2012-12, Vol.171 (12), p.1775-1785

2012

Volltextzugriff (PDF)

Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristics

Klinische Padiatrie, 2010-11, Vol.222 (6), p.356-361

2010

Volltextzugriff (PDF)

High mortality of infant bacteraemia clinically indistinguishable from severe malaria

QJM, 2004-09, Vol.97 (9), p.591-597

2004

Volltextzugriff (PDF)

Molekulargenetische Diagnostik erblicher Fiebersyndrome: Familiäres Mittelmeerfieber (FMF), Hyperimmunglobulin-D-Syndrom (HIDS), TNF-rezeptorassoziiertes periodisches Syndrom (TRAPS), Cryopyrin-assoziiertes periodisches Syndrom (CAPS: FCAS, MWS, NOMID/CINCA)

Zeitschrift für Rheumatologie, 2009-11, Vol.68 (9), p.720-725

2009

Volltextzugriff (PDF)

Molekulargenetische Diagnostik erblicher Fiebersyndrome: Familiäres Mittelmeerfieber (FMF), Hyperimmunglobulin-D-Syndrom (HIDS), TNF-rezeptorassoziiertes periodisches Syndrom (TRAPS), Cryopyrin-assoziiertes periodisches Syndrom (CAPS: FCAS, MWS, NOMID/CINCA) : Autoinflammation

Zeitschrift für Rheumatologie, 2009, Vol.68 (9)

2009

Volltextzugriff (PDF)

Cutaneous pathology in onchocerciasis associated with pronounced systemic T-helper 2-type responses to Onchocerca volvulus

British journal of dermatology (1951), 2003-10, Vol.149 (4), p.782-787

2003

Volltextzugriff (PDF)

Molecular diagnostics of hereditary fever syndromes. Familial Mediterranean fever (FMF), hyperimmunoglobulin D syndrome (HIDS), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndrome (CAPS: FCAS, MWS, NOMID/CINCA)

Zeitschrift für Rheumatologie, 2009-11, Vol.68 (9), p.720-725

2009

Volltextzugriff (PDF)

Promoter haplotypes of the interleukin-10 gene influence proliferation of peripheral blood cells in response to helminth antigen

Genes and immunity, 2004-06, Vol.5 (4), p.256-260

2004

Volltextzugriff (PDF)

Pre-treatment with chloroquine and parasite chloroquine resistance in Ghanaian children with severe malaria

QJM : An International Journal of Medicine, 2005-11, Vol.98 (11), p.789-796

2005

Volltextzugriff (PDF)

Hereditäre Fiebersyndrome

Medizinische Genetik, 2012-09, Vol.24 (3), p.211-222

2012

Volltextzugriff (PDF)

Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte function

Clinical and experimental immunology, 2005-01, Vol.139 (1), p.127-131

2005

Volltextzugriff (PDF)

FCGR2A functional genetic variant associated with susceptibility to severe malarial anaemia in Ghanaian children

Journal of medical genetics, 2010-07, Vol.47 (7), p.471-475

2010

Volltextzugriff (PDF)

Two additional human serum proteins structurally related to complement factor H. Evidence for a family of factor H-related genes

The Journal of immunology (1950), 1992-05, Vol.148 (10), p.3313-3318

1992

Volltextzugriff (PDF)

Molecular diagnostics of hereditary fever syndromes. Familial Mediterranean fever (FMF), hyperimmunoglobulin D syndrome (HIDS), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndrome (CAPS: FCAS, MWS, NOMID/CINCA)

Zeitschrift für Rheumatologie, 2009-11, Vol.68 (9), p.720

2009

Volltextzugriff (PDF)

Human Genetic Resistance to Onchocerca volvulus: Evidence for Linkage to Chromosome 2p from an Autosome-Wide Scan

The Journal of infectious diseases, 2008-08, Vol.198 (3), p.427-433

2008

Volltextzugriff (PDF)

Selection for deafness?

Nature medicine, 2002-12, Vol.8 (12), p.1332-1333

2002

Volltextzugriff (PDF)

Onchocerca volvulus-Exposed Persons Fail to Produce Interferon-γ in Response to O. volvulus Antigen but Mount Proliferative Responses with Interleukin-5 and IL-13 Production that Decrease with Increasing Microfilarial Density

The Journal of infectious diseases, 2002-04, Vol.185 (8), p.1148-1154

2002

Volltextzugriff (PDF)

Tropenmedizin in Klinik und Praxis

4., komplett überarbeitete und erweiterte Auflage.

Volltextzugriff (PDF)

Promoter Polymorphism of the Anion-Exchange Protein 1 Associated with Severe Malarial Anemia and Fatality

The Journal of infectious diseases, 2006-10, Vol.194 (7), p.949-957

2006

Volltextzugriff (PDF)

Genotyping of Plasmodium falciparum Pyrimethamine Resistance by Matrix-Assisted Laser Desorption-Ionization Time-of-Flight Mass Spectrometry

Antimicrobial Agents and Chemotherapy, 2004-02, Vol.48 (2), p.466-472

2004

Volltextzugriff (PDF)

Diagnosis of alpha+-thalassemias by determining the ratio of the two alpha-globin gene copies by oligonucleotide hybridization and melting curve analysis

Clinical chemistry (Baltimore, Md.), 2005-09, Vol.51 (9), p.1711-1713

2005

Volltextzugriff (PDF)

Dermatopathology: Cutaneous pathology in onchocerciasis associated with pronounced systemic T-helper 2-type responses to Onchocerca volvulus

British journal of dermatology (1951), 2003-10, Vol.149 (4), p.782-787

2003

Volltextzugriff (PDF)

Familial Mediterranean fever with amyloidosis associated with novel exon 2 mutation (S1791) of the MEFV gene

Blood cells, molecules, & diseases, 2003-11, Vol.31 (3), p.320-323

2003

Volltextzugriff (PDF)

1 – 25 von 156

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(142)
Mit Volltextzugriff
(124)

Publikationsform

Sprache

Englisch
(127)
Deutsch
(28)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(98)
Humans
(92)
Life Sciences & Biomedicine
(92)
Male
(74)
Female
(71)
Neurosciences & Neurology
(68)
Adult
(59)
Biological And Medical Sciences
(51)
Middle Aged
(50)
Neurosciences
(47)
Medical Sciences
(39)
Cerebellum
(38)
Clinical Neurology
(35)
Neurology
(33)
Aged
(31)
Adolescent
(25)
Child
(24)
Fundamental And Applied Biological Sciences. Psychology
(18)
Magnetic Resonance Imaging
(16)
Cerebellum - Physiology
(15)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics

Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children

Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population

Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristics

High mortality of infant bacteraemia clinically indistinguishable from severe malaria

Molekulargenetische Diagnostik erblicher Fiebersyndrome: Familiäres Mittelmeerfieber (FMF), Hyperimmunglobulin-D-Syndrom (HIDS), TNF-rezeptorassoziiertes periodisches Syndrom (TRAPS), Cryopyrin-assoziiertes periodisches Syndrom (CAPS: FCAS, MWS, NOMID/CINCA)

Molekulargenetische Diagnostik erblicher Fiebersyndrome: Familiäres Mittelmeerfieber (FMF), Hyperimmunglobulin-D-Syndrom (HIDS), TNF-rezeptorassoziiertes periodisches Syndrom (TRAPS), Cryopyrin-assoziiertes periodisches Syndrom (CAPS: FCAS, MWS, NOMID/CINCA) : Autoinflammation

Cutaneous pathology in onchocerciasis associated with pronounced systemic T-helper 2-type responses to Onchocerca volvulus

Molecular diagnostics of hereditary fever syndromes. Familial Mediterranean fever (FMF), hyperimmunoglobulin D syndrome (HIDS), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndrome (CAPS: FCAS, MWS, NOMID/CINCA)

Promoter haplotypes of the interleukin-10 gene influence proliferation of peripheral blood cells in response to helminth antigen

Pre-treatment with chloroquine and parasite chloroquine resistance in Ghanaian children with severe malaria

Hereditäre Fiebersyndrome

Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte function

FCGR2A functional genetic variant associated with susceptibility to severe malarial anaemia in Ghanaian children

Two additional human serum proteins structurally related to complement factor H. Evidence for a family of factor H-related genes

Molecular diagnostics of hereditary fever syndromes. Familial Mediterranean fever (FMF), hyperimmunoglobulin D syndrome (HIDS), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndrome (CAPS: FCAS, MWS, NOMID/CINCA)

Human Genetic Resistance to Onchocerca volvulus: Evidence for Linkage to Chromosome 2p from an Autosome-Wide Scan

Selection for deafness?

Onchocerca volvulus-Exposed Persons Fail to Produce Interferon-γ in Response to O. volvulus Antigen but Mount Proliferative Responses with Interleukin-5 and IL-13 Production that Decrease with Increasing Microfilarial Density

Tropenmedizin in Klinik und Praxis

Promoter Polymorphism of the Anion-Exchange Protein 1 Associated with Severe Malarial Anemia and Fatality

Genotyping of Plasmodium falciparum Pyrimethamine Resistance by Matrix-Assisted Laser Desorption-Ionization Time-of-Flight Mass Spectrometry

Diagnosis of alpha+-thalassemias by determining the ratio of the two alpha-globin gene copies by oligonucleotide hybridization and melting curve analysis

Dermatopathology: Cutaneous pathology in onchocerciasis associated with pronounced systemic T-helper 2-type responses to Onchocerca volvulus

Familial Mediterranean fever with amyloidosis associated with novel exon 2 mutation (S1791) of the MEFV gene

Suchergebnisse filtern