1.

Record Nr.

UNINA990009275560403321

Autore

Istituto geografico militare

Titolo

Faenza [Documento cartografico] / Istituto geografico militare

Pubbl/distr/stampa

Firenze : Istituto Geografico militare, 1987

Descrizione fisica

1 carta : color. ; 64 x 45 cm su foglio 89 x 60 cm

Collana

Carta topografica d'Italia , Serie 50 , Serie M 792 ; 239

Locazione

ILFGE

Collocazione

MP Cass.1 50 (239)

Lingua di pubblicazione

Italiano

Formato

Materiale cartografico a stampa

Livello bibliografico

Monografia

Note generali

Sulle ricognizioni parziali del 1982

2.

Record Nr.

UNINA9910557223103321

Autore

Gouw Arvin M

Titolo

Applying Next Generation Sequencing and Transgenic Models to Rare Disease Research

Pubbl/distr/stampa

Frontiers Media SA, 2020

Descrizione fisica

1 online resource (119 p.)

Soggetti

Medical genetics

Science: general issues

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Sommario/riassunto

A rare disease is a disease that occurs infrequently in the general population, typically affecting fewer than 200,000 Americans at any



given time. More than 30 million people in the United States of America (USA) and 350 million people globally suffer from rare diseases. Out of the 7000+ known rare diseases, less than 5% have approved treatments. Rare diseases are frequently chronic, progressive, degenerative, and life-threatening, compromising the lives of patients by loss of autonomy. In the USA, it can take years for a rare disease patient to receive a correct diagnosis. The socioeconomic burden for rare disease is huge. For those living with diagnosed rare diseases, there is no support system or resource bank for navigating financial, educational, or other aspects of having a rare disease. The purpose of this Research Topic is to bring together leading researchers, non-profit organizations, healthcare providers/diagnostic companies, and pharma/biotech/CROs in the field to provide a broad perspective on the latest advances, challenges, and opportunities in rare disease research.