✦ LIBER ✦

Main clues in the pathologic diagnosis of melanoma: is molecular genetics helping?

✍ Scribed by Ferrara, Gerardo; Senetta, Rebecca; Paglierani, Milena; Massi, Daniela

Book ID: 119855240
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 831 KB
Volume: 25
Category: Article
ISSN: 1396-0296
DOI: 10.1111/j.1529-8019.2012.01485.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Is sphincter electromyography a helpful

Is sphincter electromyography a helpful investigation in the diagnosis of multiple system atrophy? A retrospective study with pathological diagnosis

✍ Dominic C. Paviour; David Williams; Clare J. Fowler; Niall P. Quinn; Andrew J. L 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 62 KB

## Abstract Sphincter electromyography (spEMG) is often used as an ancillary test when multiple system atrophy (MSA) is suspected. Our aim was to determine the clinical features associated with spEMG being performed, the influence of the result on the final clinical diagnosis, and its utility as a

The Impact of Advances in Molecular Gene

The Impact of Advances in Molecular Genetic Pathology on the Classification, Diagnosis and Treatment of Selected Soft Tissue Tumors of the Head and Neck

✍ Joaquín J. García; Andrew L. Folpe 📂 Article 📅 2010 🏛 Springer US 🌐 English ⚖ 522 KB

Polar body genetic diagnosis (PbGD) is a

Polar body genetic diagnosis (PbGD) is a useful tool to improve the results of assisted reproductive technology (ART) and helps couples in their reproductive decisions

✍ J.A. Crosby; C. Fabres; E. Fernandez; A. Mackenna; Y. Triantafilo; F. Zegers-Hoc 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 86 KB

Cytogenetic and molecular genetic analys

Cytogenetic and molecular genetic analysis of primary tumours and cell lines indicate that mutation or deletion of the MTS-1 gene is a rare event in uveal melanoma

✍ A. de Klein; E. v. Drunen; G. Luyten; R. Aliredjo; N. Gruis; A. Hagemeijer 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 76 KB

Molecular Analysis of the Cyclic AMP-Dep

Molecular Analysis of the Cyclic AMP-Dependent Protein Kinase A (PKA) Regulatory Subunit 1A (PRKAR1A) Gene in Patients with Carney Complex and Primary Pigmented Nodular Adrenocortical Disease (PPNAD) Reveals Novel Mutations and Clues For Pathophysiology: Augmented PKA Signaling is Associated with Adrenal Tumorigenesis in PPNAD

✍ Lionel Groussin; Lawrence S. Kirschner; Caroline Vincent-Dejean; Karine Perlemoi 📂 Article 📅 2002 🏛 American Society of Human Genetics 🌐 English ⚖ 913 KB