Pathology, Laboratory Medicine and Forensic Medicine

Hypertext atlas of Neonatal Pathology

Hypertext Atlas of Neonatal Pathology contains clinical and histological images of various forms of neonatal pathology. Virtual microscope interface is used to access histological images available in very high resolution. The Atlas is available in English and Czech.

author: MUDr. Marta Ježová, MUDr. Sylva Hotárková, MUDr. Katarína Múčková, MUDr. Ondřej Souček, MUDr. Pavel Vlašín, doc. MUDr. Josef Feit, CSc. | LF MU | discipline: Anatomy, Pathology, Laboratory Medicine and Forensic Medicine, Paediatrics, Neonatology | category: Multimedia, Educational websites | keywords: neonatology, foetus, neonatal, foetal, newborn, pregnancy | attachment: 1 | viewed: 81x | published on: 27.1.2010 | last modified on: 2.2.2010

Hypertext atlas of Rare Lymphomas

Hypertext Atlas of Rare Lymphomas contains clinical and histological images of some rare hematologic/lymphatic malignancies of children. Virtual microscope interface is used to access histological images available in very high resolution. The Atlas is available in English and Czech.

Random access analyser (HITACHI 917)

The automatic biochemical analyser Hitachi 917 is a prototype of high-capacity selective analyser. The duration of the video is 17 min.

Hypertext atlas of Dermatopathology

Hypertext Atlas of Dermatopathology contains thousands of clinical and histological images of skin diseases. Virtual microscope interface is used to access histological images available in very high resolution. The Atlas is available in English and Czech.

author: Assoc.Prof. MUDr. Josef Feit, CSc., Hana Jedličková, Zdeněk Vlašín, Günter Burg, Werner Kempf, Luděk Matyska | LF MU | discipline: Dermatology, Pathology, Laboratory Medicine and Forensic Medicine | category: Multimedia, Educational websites | keywords: non-tumorous skin diseases, skin tumors, cysts of the skin and subcutis, dermatovenerology | attachment: 1 | viewed: 977x | published on: 17.4.2008 | last modified on: 2.2.2010

Hypertext atlas of Pathology

Hypertext Atlas of Organ Pathology contains teaching materials for pre-graduate students. It is under construction and in full version so far available in Czech language only. The English version contains only chapters with images to enable image sharing (see bellow). The interface is similar to the Atlas of Dermatopathology. Many macroscopic and microscopic images are available, as well as images from CT and MRI scanners and endoscopes.

Hypertext atlas of Bone Marrow Pathology

Hypertext Atlas of Bone Marrow Pathology Pathology contains clinical and histological images of various forms of bone marrow diseases. Virtual microscope interface is used to access histological images available in very high resolution. The Atlas is available in English and Czech.

Hypertext atlas of Fetal Pathology

Hypertext Atlas of Fetal and Neonatal Pathology contains clinical and histological images of various form of developmental anomalies. Virtual microscope interface is used to access histological images available in very high resolution. The Atlas is available in English and Czech.

author: MUDr. Marta Ježová, MUDr. Sylva Hotárková, MUDr. Katarína Múčková, MUDr. Ondřej Souček, MUDr. Pavel Vlašín, doc. MUDr. Josef Feit, CSc. | LF MU | discipline: Anatomy, Pathology, Laboratory Medicine and Forensic Medicine, Paediatrics, Neonatology | category: Multimedia, Educational websites | keywords: neonatology, foetopathology, foetus, neonatal, foetal, newborn, pregnancy | attachment: 2 | viewed: 1047x | published on: 17.4.2008 | last modified on: 2.2.2010

Atypical phenotype of Dubin-Johnson syndrome caused by co-inherited defects in two crucial genes of bilirubin excretory pathway: A

Úvod: Dubin-Johnsonův syndrom je autosomálně resesivně dědičná převářně nekonjugovaná hyperbilirubinémie vyvolaná mutacemi v genu ABCC2/MRP2 kódujícím kanalikulární transportér pro konjugovaný bilirubin. Gilbertův syndrom je recesivně dědičná nekonjugovaná hyperbilirubinémie vyvolaná ve většině případů sníženou aktivitou transkripce genu UGT1A1 v důsledku homozygotní mutace A(TA)7TAA v promotoru uvedeného genu. Cílem naší studie bylo najít molekulární příčinu atypické intermitentní převážně nekonjugované hyperbilirubinémie u 3-letého chlapce. Metody: Žlučové cesty byly zobrazeny cholescintigrafií s použitím 99mTc-HIDA. Exprese proteinu ABCC2/MRP2 byla vyšetřena imunohistologicky. Sekvence genů UGT1A1 a ABCC2/MRP2 byla určena přímým sekvenováním z genomové DNA. Přítomnost nalezených mutací byla potvrzena fragmentovou analýzou, sekvenováním klonovaných fragmenů genomové DNA s mutací a PCR-RFLP....

author: Milan Elleder, Dita Cebecauerová, Tomáš Jirásek, Lucie Budišová, Václav Mandys, Vladimír Volf, Zorka Novotná, Iva Subhanová, Martin Hřebíček, Milan Elleder, Milan Jirsa | 1.LF UK | discipline: Biochemistry, Chemistry, Gastroenterology and Hepatology, Genetics, Pathology, Laboratory Medicine and Forensic Medicine, Paediatrics, Neonatology | category: E-learning objects archive | keywords: Dubin-Johnsonův syndrom, Gilbertův syndrom, ABCC2/MRP2, UGT1A1 | attachment: 1 | viewed: 2094x | published on: 2.1.2007 | last modified on: 4.7.2006