UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 382

Sortiert nach

Long-Term Efficacy and Safety of Pegvisomant in Combination With Long-Acting Somatostatin Analogs in Acromegaly

The journal of clinical endocrinology and metabolism, 2014-10, Vol.99 (10), p.3644-3652

2014

Link zum Volltext

Verfügbarkeit prüfen

Afamelanotide for Erythropoietic Protoporphyria

The New England journal of medicine, 2015-07, Vol.373 (1), p.48-59

2015

Link zum Volltext

Verfügbarkeit prüfen

Common variants in PCSK1 influence blood pressure and body mass index

Journal of human hypertension, 2015-02, Vol.29 (2), p.82-86

2015

Link zum Volltext

Verfügbarkeit prüfen

Porphyrin biosynthesis in human Barrett's oesophagus and adenocarcinoma after ingestion of 5-aminolaevulinic acid

British journal of cancer, 2000-08, Vol.83 (4), p.539-543

2000

Link zum Volltext

Verfügbarkeit prüfen

HDL associates with insulin resistance and beta-cell dysfunction in South Asian families at risk of type 2 diabetes

Journal of diabetes and its complications, 2021-10, Vol.35 (10), p.107993, Article 107993

2021

Link zum Volltext

Verfügbarkeit prüfen

Vitamin D deficiency in patients with erythropoietic protoporphyria

Journal of inherited metabolic disease, 2010-12, Vol.33 (Suppl 3), p.1-4

2010

Link zum Volltext

Verfügbarkeit prüfen

Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

Clinical genetics, 2007-12, Vol.72 (6), p.568-573

2007

Link zum Volltext

Verfügbarkeit prüfen

High cancer risk and increased mortality in patients with Peutz–Jeghers syndrome

Gut, 2011-02, Vol.60 (2), p.141-147

2011

Link zum Volltext

Verfügbarkeit prüfen

A Gly15Arg Mutation in the Interleukin-10 Gene Reduces Secretion of Interleukin-10 in Crohn Disease

Scandinavian journal of gastroenterology, 2003-01, Vol.38 (6), p.611-617

2003

Link zum Volltext

Verfügbarkeit prüfen

Allele-sharing of cytokine genes in familial inflammatory bowel disease

Hepato-gastroenterology, 2007-07, Vol.54 (77), p.1467

2007

Link zum Volltext

Verfügbarkeit prüfen

Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in The Netherlands

Cellular and molecular biology (Noisy-le-Grand, France), 2009-07, Vol.55 (2), p.64

2009

Link zum Volltext

Verfügbarkeit prüfen

STRAD in Peutz-Jeghers syndrome and sporadic cancers

Journal of clinical pathology, 2005-10, Vol.58 (10), p.1091-1095

2005

Link zum Volltext

Verfügbarkeit prüfen

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

Journal of medical genetics, 2006-05, Vol.43 (5), p.e18-e18

2006

Link zum Volltext

Verfügbarkeit prüfen

Nasal polyposis in Peutz–Jeghers syndrome: a distinct histopathological and molecular genetic entity

Journal of clinical pathology, 2007-04, Vol.60 (4), p.392-396

2007

Link zum Volltext

Verfügbarkeit prüfen

Acrylate yellow filters in operating lights protect against photosensitization tissue damage

British journal of surgery, 2000-02, Vol.87 (2), p.231-235

2000

Link zum Volltext

Verfügbarkeit prüfen

Biochemical basis of 5-aminolaevulinic acid-induced protoporphyrin IX accumulation: a study in patients with (pre)malignant lesions of the oesophagus

British journal of cancer, 1998-09, Vol.78 (5), p.679-682

1998

Link zum Volltext

Verfügbarkeit prüfen

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

British journal of cancer, 2005-03, Vol.92 (6), p.1126-1129

2005

Link zum Volltext

Verfügbarkeit prüfen

Peutz-Jeghers syndrome: 78-year follow-up of the original family

The Lancet (British edition), 1999-04, Vol.353 (9160), p.1211-1215

1999

Link zum Volltext

Verfügbarkeit prüfen

A functional interleukin-10 mutation in Dutch patients with Crohn's disease

Digestive and liver disease, 2005-05, Vol.37 (5), p.330-335

2005

Link zum Volltext

Verfügbarkeit prüfen

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndrome

British journal of cancer, 2005-03, Vol.92 (6), p.1126-1129

2005

Link zum Volltext

Verfügbarkeit prüfen

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRAD , and MO25 , in Peutz-Jeghers syndrome

British journal of cancer, 2005-03, Vol.92 (6), p.1126-1129

2005

Link zum Volltext

Verfügbarkeit prüfen

Residual activity of human porphobilinogen deaminase with R167Q or R167W mutations: an explanation for survival of homozygous and compound heterozygous acute intermittent porphyrics

Cellular and molecular biology (Noisy-le-Grand, France), 2002-12, Vol.48 (8), p.861

2002

Link zum Volltext

Verfügbarkeit prüfen

Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyria

Journal of inherited metabolic disease, 1990-09, Vol.13 (5), p.684-686

1990

Link zum Volltext

Verfügbarkeit prüfen

Two course illuminating scheme improves aminolevulinic acid photodynamic therapy in cell cultures

Cellular and molecular biology (Noisy-le-Grand, France), 2002-12, Vol.48 (8), p.903

2002

Link zum Volltext

Verfügbarkeit prüfen

Kinetics, localization, and mechanism of 5-aminolevulinic acid-induced porphyrin accumulation in normal and Barrett's-like rat esophagus

Lasers in surgery and medicine, 1999, Vol.24 (1), p.3-13

1999

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 382

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(354)
Mit Volltextzugriff
(336)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(297)
Life Sciences & Biomedicine
(221)
Humans
(195)
Male
(126)
Female
(124)
Aged
(82)
Middle Aged
(81)
Biological And Medical Sciences
(62)
Adult
(61)
Medical Sciences
(55)
Physical Sciences
(49)
Risk Factors
(48)
Neurosciences & Neurology
(46)
Technology
(42)
Treatment Outcome
(35)
Physics
(33)
Clinical Neurology
(32)
Medicin Och Hälsovetenskap
(30)
Science & Technology - Other Topics
(30)
Prospective Studies
(29)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Long-Term Efficacy and Safety of Pegvisomant in Combination With Long-Acting Somatostatin Analogs in Acromegaly

Afamelanotide for Erythropoietic Protoporphyria

Common variants in PCSK1 influence blood pressure and body mass index

Porphyrin biosynthesis in human Barrett's oesophagus and adenocarcinoma after ingestion of 5-aminolaevulinic acid

HDL associates with insulin resistance and beta-cell dysfunction in South Asian families at risk of type 2 diabetes

Vitamin D deficiency in patients with erythropoietic protoporphyria

Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

High cancer risk and increased mortality in patients with Peutz–Jeghers syndrome

A Gly15Arg Mutation in the Interleukin-10 Gene Reduces Secretion of Interleukin-10 in Crohn Disease

Allele-sharing of cytokine genes in familial inflammatory bowel disease

Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in The Netherlands

STRAD in Peutz-Jeghers syndrome and sporadic cancers

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

Nasal polyposis in Peutz–Jeghers syndrome: a distinct histopathological and molecular genetic entity

Acrylate yellow filters in operating lights protect against photosensitization tissue damage

Biochemical basis of 5-aminolaevulinic acid-induced protoporphyrin IX accumulation: a study in patients with (pre)malignant lesions of the oesophagus

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

Peutz-Jeghers syndrome: 78-year follow-up of the original family

A functional interleukin-10 mutation in Dutch patients with Crohn's disease

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndrome

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRAD , and MO25 , in Peutz-Jeghers syndrome

Residual activity of human porphobilinogen deaminase with R167Q or R167W mutations: an explanation for survival of homozygous and compound heterozygous acute intermittent porphyrics

Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyria

Two course illuminating scheme improves aminolevulinic acid photodynamic therapy in cell cultures

Kinetics, localization, and mechanism of 5-aminolevulinic acid-induced porphyrin accumulation in normal and Barrett's-like rat esophagus

Suchergebnisse filtern