UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 459

Sortiert nach

An ex vivo RNA trans‐splicing strategy to correct human generalized severe epidermolysis bullosa simplex

British journal of dermatology (1951), 2019-01, Vol.180 (1), p.141-148

2019

Volltextzugriff (PDF)

Ethical and Predatory Publishing: Experiences and Perceptions of Researchers

Bulletin of the Transilvania University of Brașov. Series VII, Social sciences, law, 2017-01, Vol.10 (2), p.55-66

2017

Volltextzugriff (PDF)

Acute keratoconus with perforation in a patient with Down’s syndrome

British journal of ophthalmology, 2003-01, Vol.87 (1), p.120-120

2003

Volltextzugriff (PDF)

Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

Journal of cutaneous pathology, 2003-10, Vol.30 (9), p.553-560

2003

Volltextzugriff (PDF)

Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosa

British journal of dermatology (1951), 2006-01, Vol.154 (1), p.185-187

2006

Volltextzugriff (PDF)

Cerebral Localized Marginal Zone Lymphoma Presenting as Hypothalamic-Pituitary Region Disorder

Case reports in neurology, 2011-05, Vol.3 (2), p.129-135

2011

Volltextzugriff (PDF)

Elemental Analysis in Electron Microscopy for Medical Diagnostics

Microscopy and microanalysis, 2007-09, Vol.13 (S03), p.222-223

2007

Volltextzugriff (PDF)

Routine, rapid, noninvasive diagnosis of viral skin exanthems

British journal of dermatology (1951), 2006-03, Vol.154 (3), p.558-560

2006

Volltextzugriff (PDF)

P.159Disease spectrum in nemaline myopathy due to LMOD3 mild founder mutation in Austria and southern Germany

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S94-S95

2019

Volltextzugriff (PDF)

Joint Meeting of the Society for Cutaneous Ultrastructure Research (31st Annual Meeting of SCUR) with the European Society for Dermatopathology (ESDP) and V Incontro Clinico Patologico Romano 6th–8th May 2004 ROME, Italy

Journal of investigative dermatology, 2004-11, Vol.123 (5), p.A87-A97

2004

Volltextzugriff (PDF)

Ocular involvement in IgA–epidermolysis bullosa acquisita

British journal of dermatology (1951), 1999-11, Vol.141 (5), p.887-892

1999

Volltextzugriff (PDF)

169 Regeneration of a functional epidermis at a large, long-standing wound by gene-corrected autologous epidermal stem cells

Journal of investigative dermatology, 2016-09, Vol.136 (9), p.S189-S189

2016

Volltextzugriff (PDF)

Gene symbol: Kind1. Disease: kindler syndrome

Human genetics, 2004-07, Vol.115 (2), p.175-175

2004

Volltextzugriff (PDF)

Recurrent Keratoconus in a Patient with Leber Congenital Amaurosis

Cornea, 2000-05, Vol.19 (3), p.395-398

2000

Volltextzugriff (PDF)

Distribution of two VIP-related peptides, helospectin and pituitary adenylate cyclase activating peptide (PACAP), in the human upper respiratory system

Regulatory peptides, 1996-09, Vol.65 (3), p.203-209

1996

Volltextzugriff (PDF)

Light and transmission electron microscopic studies following frontal sinus obliteration with ionomer cement in cats

European archives of oto-rhino-laryngology, 1995-09, Vol.252 (6), p.332-335

1995

Volltextzugriff (PDF)

Amnion-Limbus-Transplantation zur Oberflächenrekonstruktion nach schwerer Verätzung und Verbrennung

Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft, 2002, Vol.99 (11), p.839-848

2002

Volltextzugriff (PDF)

Modern Analytical Electron Microscopical Methods for Confirmation of Previously Suspected – Morphologically Established – Ultrastructural Diagnosis of an “Inflammatory Myopathy” in Human Skeletal Muscle Tissue: “Macrophagic Myofasciitis”

Microscopy and microanalysis, 2007-09, Vol.13 (S03), p.180-181

2007

Volltextzugriff (PDF)

Routine, rapid, noninvasive diagnosis of viral skin exanthems: Correspondence

British journal of dermatology (1951), 2006-03, Vol.154 (3), p.558-560

2006

Volltextzugriff (PDF)

Autonomic and Peptidergic Innervation of Human Nasal Mucosa

Acta oto-laryngologica, 1993, Vol.113 (3), p.387-393

1993

Volltextzugriff (PDF)

Annual Meeting of the Society for Cutaneous Ultrastructure Research (34th Annual Meeting of SCUR)

Journal of investigative dermatology, 2008-03, Vol.128 (3), p.759-763

2008

Volltextzugriff (PDF)

Die autonome und peptiderge Innervation des menschlichen Kehlkopfes

HNO, 1994, Vol.42 (2), p.89-98

1994

Volltextzugriff (PDF)

Diaminobenzidine as a myelin stain in semithin plastic sections

Biotechnic & histochemistry, 2000-01, Vol.75 (1), p.46-47

Muss, W

2000

Volltextzugriff (PDF)

A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance

Neuromuscular disorders : NMD, 2006-12, Vol.16 (12), p.874-877

2006

Volltextzugriff (PDF)

A Compound Heterozygous One Amino-Acid Insertion/Nonsense Mutation in the Plectin Gene Causes Epidermolysis Bullosa Simplex with Plectin Deficiency

The American journal of pathology, 2001-02, Vol.158 (2), p.617-625

2001

Volltextzugriff (PDF)

1 – 25 von 459

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(206)
Mit Volltextzugriff
(430)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(125)
Life Sciences & Biomedicine
(122)
Humans
(116)
Female
(86)
Oncology
(75)
Middle Aged
(68)
Biological And Medical Sciences
(65)
Aged
(60)
Medical Sciences
(59)
Adult
(55)
Recent Theological Literature
(46)
Male
(33)
Chemotherapy
(32)
Breast Neoplasms - Drug Therapy
(30)
History
(30)
Breast Cancer
(27)
Tumors
(24)
Antineoplastic Combined Chemotherapy Protocols - Therapeutic Use
(23)
Pharmacology. Drug Treatments
(23)
Antineoplastic Agents
(21)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

An ex vivo RNA trans‐splicing strategy to correct human generalized severe epidermolysis bullosa simplex

Ethical and Predatory Publishing: Experiences and Perceptions of Researchers

Acute keratoconus with perforation in a patient with Down’s syndrome

Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosa

Cerebral Localized Marginal Zone Lymphoma Presenting as Hypothalamic-Pituitary Region Disorder

Elemental Analysis in Electron Microscopy for Medical Diagnostics

Routine, rapid, noninvasive diagnosis of viral skin exanthems

P.159Disease spectrum in nemaline myopathy due to LMOD3 mild founder mutation in Austria and southern Germany

Joint Meeting of the Society for Cutaneous Ultrastructure Research (31st Annual Meeting of SCUR) with the European Society for Dermatopathology (ESDP) and V Incontro Clinico Patologico Romano 6th–8th May 2004 ROME, Italy

Ocular involvement in IgA–epidermolysis bullosa acquisita

169 Regeneration of a functional epidermis at a large, long-standing wound by gene-corrected autologous epidermal stem cells

Gene symbol: Kind1. Disease: kindler syndrome

Recurrent Keratoconus in a Patient with Leber Congenital Amaurosis

Distribution of two VIP-related peptides, helospectin and pituitary adenylate cyclase activating peptide (PACAP), in the human upper respiratory system

Light and transmission electron microscopic studies following frontal sinus obliteration with ionomer cement in cats

Amnion-Limbus-Transplantation zur Oberflächenrekonstruktion nach schwerer Verätzung und Verbrennung

Modern Analytical Electron Microscopical Methods for Confirmation of Previously Suspected – Morphologically Established – Ultrastructural Diagnosis of an “Inflammatory Myopathy” in Human Skeletal Muscle Tissue: “Macrophagic Myofasciitis”

Routine, rapid, noninvasive diagnosis of viral skin exanthems: Correspondence

Autonomic and Peptidergic Innervation of Human Nasal Mucosa

Annual Meeting of the Society for Cutaneous Ultrastructure Research (34th Annual Meeting of SCUR)

Die autonome und peptiderge Innervation des menschlichen Kehlkopfes

Diaminobenzidine as a myelin stain in semithin plastic sections

A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance

A Compound Heterozygous One Amino-Acid Insertion/Nonsense Mutation in the Plectin Gene Causes Epidermolysis Bullosa Simplex with Plectin Deficiency

Suchergebnisse filtern