UB Paderborn / Katalog / Suche / in CDI

1 – 16 von 16

Sortiert nach

Recombinant Encapsulated Cells Overexpressing Alpha-L-Iduronidase Correct Enzyme Deficiency in Human Mucopolysaccharidosis Type I Cells

Cells, tissues, organs, 2012-01, Vol.195 (4), p.323-329

2012

Link zum Volltext

Verfügbarkeit prüfen

Azurophilic inclusions in lymphocytes and plasma cells: a case of Sanfilippo disease

British journal of haematology, 2014-03, Vol.164 (5), p.618-618

2014

Link zum Volltext

Verfügbarkeit prüfen

Molecular Demonstration of SLC4A1 Gene Deletion in Two Mexican Patients with Southeast Asian Ovalocytosis

Human biology, 2005-06, Vol.77 (3), p.399-405

2005

Link zum Volltext

Verfügbarkeit prüfen

DIFFERENTIAL EXPRESSION OF CALRETICULIN IN DEVELOPMENTAL STAGES OF TAENIA SOLIUM

The Journal of parasitology, 2006-08, Vol.92 (4), p.789-795

2006

Link zum Volltext

Verfügbarkeit prüfen

From stillness to motion: 80 years after the first description of Taenia solium oncosphere hatching

Parasites & vectors, 2014-01, Vol.7 (1), p.12-12, Article 12

2014

Link zum Volltext

Verfügbarkeit prüfen

Next-generation sequencing and high-throughput enzymolome-based panel screening of suspected lysosomal disease cases identifies multiple disease-causing variants in two genes underlying different lysosomal diseases: A source of clinical and metabolic variability?

Molecular genetics and metabolism, 2023-02, Vol.138 (2), p.107072, Article 107072

2023

Link zum Volltext

Verfügbarkeit prüfen

Diagnosis of 4 novel cases of adult acid sphyngomielynase deficiency by screening with next-generation sequencing gene panels

Molecular genetics and metabolism, 2020-02, Vol.129 (2), p.S156-S156

2020

Link zum Volltext

Verfügbarkeit prüfen

Genetic screening of lysosomal disorders: An account of five years' experience with NGS-based resequencing panels

Molecular genetics and metabolism, 2022-02, Vol.135 (2), p.S36-S36

2022

Link zum Volltext

Verfügbarkeit prüfen

Efficiency of NGS-based gene panels as first-line screening tests for the diagnosis of lysosomal diseases

Molecular genetics and metabolism, 2020-02, Vol.129 (2), p.S47-S47

2020

Link zum Volltext

Verfügbarkeit prüfen

MACROMELANOSOMES AS MORPHOLOGIC MARKERS IN CHILDHOOD NEUROFIBROMATOSES

Pediatric dermatology, 1991-03, Vol.8 (1), p.91-93

1991

Link zum Volltext

Verfügbarkeit prüfen

Giant cytoplasmic granules in Langerhans cells of Chediak-Higashi syndrome

The American journal of dermatopathology, 1990-02, Vol.12 (1), p.81-87

1990

Link zum Volltext

Verfügbarkeit prüfen

Molecular demonstration of SLC4A1 gene deletion in two Mexican patients with Southeast Asia ovalocytosisn

Human biology, 2005-06, Vol.77 (3), p.399

2005

Link zum Volltext

Verfügbarkeit prüfen

Lymphoid papillary hyperplasia of the palatine tonsils

The American journal of surgical pathology, 1983-09, Vol.7 (6), p.579-582

1983

Link zum Volltext

Verfügbarkeit prüfen

Molecular Demonstration of SLC4A1 Gene Deletion in Two Mexican Patients with Ovalocytosis

Human biology, 2005, Vol.77 (3), p.399-405

2005

Link zum Volltext

Verfügbarkeit prüfen

Osler-Weber-Rendu disease in an infant

Human pathology, 1988-10, Vol.19 (10), p.1243-1246

1988

Link zum Volltext

Verfügbarkeit prüfen

Use of absorbable sutures in canine carotid arteries

Texas Heart Institute journal, 1990, Vol.17 (2), p.99-102

1990

Link zum Volltext

Verfügbarkeit prüfen

1 – 16 von 16

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(16)
Mit Volltextzugriff
(15)

Publikationsform

Artikel
(16)

Sprache

Englisch
(16)

Erscheinungsjahr

n.n

Thema

Humans
(9)
Life Sciences & Biomedicine
(8)
Science & Technology
(8)
Animals
(3)
Biological And Medical Sciences
(3)
Child
(3)
Infant
(3)
Cricetinae
(2)
Cysticercosis
(2)
Female
(2)
Male
(2)
Medical Sciences
(2)
Melanocytes - Pathology
(2)
Mexico
(2)
Oncospheres
(2)
Parasitology
(2)
Pathology
(2)
Taenia Solium
(2)
Taenia Solium - Growth & Development
(2)
Acidosis
(1)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Recombinant Encapsulated Cells Overexpressing Alpha-L-Iduronidase Correct Enzyme Deficiency in Human Mucopolysaccharidosis Type I Cells

Azurophilic inclusions in lymphocytes and plasma cells: a case of Sanfilippo disease

Molecular Demonstration of SLC4A1 Gene Deletion in Two Mexican Patients with Southeast Asian Ovalocytosis

DIFFERENTIAL EXPRESSION OF CALRETICULIN IN DEVELOPMENTAL STAGES OF TAENIA SOLIUM

From stillness to motion: 80 years after the first description of Taenia solium oncosphere hatching

Next-generation sequencing and high-throughput enzymolome-based panel screening of suspected lysosomal disease cases identifies multiple disease-causing variants in two genes underlying different lysosomal diseases: A source of clinical and metabolic variability?

Diagnosis of 4 novel cases of adult acid sphyngomielynase deficiency by screening with next-generation sequencing gene panels

Genetic screening of lysosomal disorders: An account of five years' experience with NGS-based resequencing panels

Efficiency of NGS-based gene panels as first-line screening tests for the diagnosis of lysosomal diseases

MACROMELANOSOMES AS MORPHOLOGIC MARKERS IN CHILDHOOD NEUROFIBROMATOSES

Giant cytoplasmic granules in Langerhans cells of Chediak-Higashi syndrome

Molecular demonstration of SLC4A1 gene deletion in two Mexican patients with Southeast Asia ovalocytosisn

Lymphoid papillary hyperplasia of the palatine tonsils

Molecular Demonstration of SLC4A1 Gene Deletion in Two Mexican Patients with Ovalocytosis

Osler-Weber-Rendu disease in an infant

Use of absorbable sutures in canine carotid arteries

Suchergebnisse filtern