✦ LIBER ✦

Segmental colitis associated with diverticula: A rare clinical entity and a new challenge for the gastroenterologist

✍ Scribed by E. Ierardi; C. Hassan; A. Zullo; V. De Francesco; N. Della Valle; S. Prencipe; R. Rosania; S. Morini; C. Panella

Book ID: 119229526
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 525 KB
Volume: 41
Category: Article
ISSN: 1590-8658
DOI: 10.1016/j.dld.2009.04.016

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Pattern of mucosal tumor necrosis factor

Pattern of mucosal tumor necrosis factor-α expression in segmental colitis associated with diverticula suggests a truly autonomous clinical entity

✍ Antonio Tursi; Cosimo Damiano Inchingolo; Rosanna Nenna; Giuseppe Stoppino; Mari 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 68 KB

Diffuse idiopathic pulmonary neuroendocr

Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia and the associated lung neuroendocrine tumors : Clinical experience with a rare entity

✍ Alexander Gorshtein; David J. Gross; Dganit Barak; Yulia Strenov; Yael Refaeli; 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 801 KB

## Abstract ## BACKGROUND: Normal adult lungs contain pulmonary neuroendocrine cells (PNECs). PNEC hyperplasia may be either reactive or idiopathic, and the idiopathic type is defined as diffuse idiopathic PNEC hyperplasia (DIPNECH). It is believed that DIPNECH is a neuroendocrine proliferative pr

A cytogenetic study of 397 consecutive a

A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity

✍ Eric Jeandidier; Carine Gervais; Isabelle Radford-Weiss; Estelle Zink; Catherine 📂 Article 📅 2012 🏛 Elsevier 🌐 English ⚖ 537 KB

The combination of bortezomib and dexame

The combination of bortezomib and dexamethasone is an efficient therapy for relapsed/refractory scleromyxedema: a rare disease with new clinical insights

✍ Javier Cañueto; Jorge Labrador; Concepción Román; Ángel Santos-Briz; Teresa Cont 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 282 KB

Rationale, design, and methods for a piv

Rationale, design, and methods for a pivotal randomized clinical trial for the assessment of a cardiac support device in patients with New York health association class III-IV heart failure

✍ Douglas L. Mann; Michael A. Acker; Mariell Jessup; Hani N. Sabbah; Randall C. St 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 274 KB

Search for mutations in a segment of the

Search for mutations in a segment of the exon 28 of the human von Willebrand factor gene: New mutations, R1315C and R1341W, associated with type 2M and 2B variants

✍ Casaña, Pilar; Martínez, Francisco; Espinós, Carmen; Haya, Saturnino; Lorenzo, J 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 431 KB 👁 1 views

von Willebrand Disease (vWD) is the most frequently inherited bleeding disorder in humans, and is caused by a qualitative and/or quantitative abnormality of the von Willebrand factor (vWF). A large number of defects that cause qualitative variants have been located in the A1 domain of the vWF, which