Albumin Serotonin Cathepsin D Fibrinogen ATP Cathepsin E Fibronectin ADP
Carboxypeptidase A Vitronectin Calcium Carboxypeptidase B Osteonectin Pyrophosphate …

Although CHS is a rare disease, the Chediak-like family of proteins is providing insight into
the regulation of vesicle trafficking. Understanding the basic mechanisms that govern vesicle …

The American Academy of Allergy, Asthma & Immunology (AAAAI) and the American
College of Allergy, Asthma & Immunology (ACAAI) have jointly accepted responsibility for …

The purpose of this Practice Parameter for the Diagnosis and Management of Primary
Immunodeficiency is to provide the consultant allergist/immunologist with a practical guide …

Chediak–Higashi syndrome (CHS) is a rare autosomal recessive disorder characterized by
variable degrees of oculocutaneous albinism, easy bruisability, and bleeding as a result of …

Hemophagocytic lymphohistiocytosis (HLH) is a rare life‐threatening disease in which the
immune system becomes overactive due to its inability to effectively respond to infections …

Patients with defects in phagocytic function are predisposed to intracellular microorganisms
and typically have early dissemination of the infection. Recognition of the underlying …

Background The treatment of chronic granulomatous disease with conventional allogeneic
hematopoietic stem-cell transplantation carries a high risk of serious complications and …

Neutrophil disorders are an uncommon yet important cause of morbidity and mortality in
infants and children. This article is an overview of these conditions, with emphasis on clinical …

Plasma membrane resealing is a Ca2+-dependent process that involves the exocytosis of
intracellular vesicles next to the wound site. Recent studies revealed that conventional …