QCD-TARO Collaboration: Irina Pushkina , Philippe de Forcrand, Margarita Garcia Perez, Seyong Kim, Hideo Matsufuru, Atsushi Nakamura , Ion-Olimpiu Stamatescu, Tetsuya Takaishi and Takashi Umeda School of Biosphere Science, Hiroshima University, Higashi-Hiroshima 739-8526, Japan b Institut für Theoretische Physik, ETH-Hönggerberg, CH-8093 Zürich, Switzerland, and Theory Division, CERN, CH-1211 G...

Chediak-Higashi syndrome is a rare autosomal recessive disorder due to a qualitative defect in leucocyte function characterized clinically by partial oculocutaneous albinism, recurrent bacterial infections, photophobia etc. The diagnostic feature is the presence of abnormal giant intracytoplasmic granules in neutrophils and their precursors. Here we report this syndrome in two siblings who pres...

Angela-Guiovana Rincón, Elizabeth León, Rodrigo Jiménez, Sandra Parra, Carlos-Andrés Peña y Cesar Pulgarín 1 Laboratory for Environmental Biotechnology, Institute of Environmental Engineering 2 Ecosystem Management Laboratory, Institute of Environmental Engineering 3 Air Pollution Laboratory (LPAS) 4 Logic systems Laboratory (LSL) Swiss Federal Institute of Technology, CHB Ecublens CH 1015 Laus...

1 Departamento de Microbiologı́a I, Inmunologı́a, Facultad de Medicina, Universidad Complutense, 28040 Madrid, Spain 2 Inmunotek SL, Alcalá de Henares, 28805 Madrid, Spain 3 School of Life and Health Sciences, Aston University, Birmingham B4 7ET, UK 4ATR, LLC, Worcester, MA 01606, USA 5Department of Mycobacteriology, National Institute of Infectious Diseases, Higashi-Murayama, Tokyo 189-0002, Japan

Chediak-Higashi syndrome (CHS), an autosomal recessive defect of polymorphonuclear leucocytic function is characterized by increased susceptibility to pyogenic infections, oculocutaneous albinism, neutropenia and presence of abnormal granules in leucocytes. This rare disorder has been described in approximately 80 cases from world over including three reports from India since its first descript...

The Chediak Higashi Syndrome (CHS) is a rare autosomal recessive disease characterized by partial oculo-cutaneous albinism, frequent pyogenic infections, presence of giant granules in leucocytes and other granule containing cells(l). To date less than 150 cases have been reported in the world literature. This includes a pregnant lady who delivered a normal child(2). The first case in India was ...

Recent ERP findings challenge the widespread assumption that syntactic and semantic processes are tightly coupled. Syntactically well-formed sentences that are semantically anomalous due to thematic mismatches elicit a P600, the component standardly associated with syntactic anomaly. This 'thematic P600' effect has been attributed to detection of semantically plausible thematic relations that c...