Results 71 to 80 of about 24,352 (312)

All‐in‐one optical microfiber with an interface for MRSA in biofilms: Integrating rapid quantitative analysis and synergistic antimicrobial therapy

open access: yesInfoMat, EarlyView.
Aiming at the management of MRSA biofilms, an all‐in‐one optical microfiber that integrated rapid quantitative analysis with synergistic antimicrobial therapy is developed. The prepared interfacial‐functionalized optical microfiber demonstrates the ability to detect MRSA concentrations in infection sites, enhance therapeutic efficacy, and assess ...
Pengwei Chen   +7 more
wiley   +1 more source

Orthotopic liver transplantation in children. Two-year experience with 47 patients [PDF]

open access: yes, 1984
During a 24-month period (May 1981 to May 1983), 47 pediatric patients (ranging in age from 7 months to 18 years) underwent orthotopic liver transplantation using cyclosporine and prednisone.
Gartner, JC   +5 more
core  

A Macrophage Phenotype for a Constitutive, Class II Antigen-Expressing, Human Dermal Perivascular Dendritic Cell [PDF]

open access: yes, 1989
A previously uncharacterized population of class II antigen-bearing dendritic cells that are intimately associated with the dermal microvasculature was identified in normal human skin using a double-label, indirect immunofluorescence technique.
Matsubara, Tsukasa   +2 more
core   +1 more source

A rare case of oral multisystem Langerhans cell histiocytosis [PDF]

open access: yes, 2017
Langerhans cell histiocytosis (LCH) is a rare disorder characterized by high proliferation of Langerhans dendritic cells. LCH is a solitary or multifocal disease that primarily involves bone tissue and often affects children and young men. A 29 years-old
Facciolo, Maria Teresa   +4 more
core   +1 more source

Langerhans cell histiocytosis: current concepts in dentistry and case report [PDF]

open access: yes, 2016
Langerhans cell histiocytosis (LCH), which is a rare granulomatous pediatric disease of unknown etiology, is characterized by the idiopathic proliferation and accumulation of abnormal and clonal Langerhans cells or their ...
Alejo-Gonzalez, Francisco   +4 more
core  

The cytogenesis of ascitic pha­gocytes [PDF]

open access: yes, 1959
Judging from our vital observation conducted mainly by tissue culture, it was firmly demonstrated that ascitic phagocytes are not histiocytes but they are the cells closely related to monocytes and that the sites of the genesis are the milky spots of the
Fukuda, Genjiro   +6 more
core   +1 more source

Liver transplantation for biliary atresia [PDF]

open access: yes, 1984
Orthotopic liver transplantation was performed 15 months to 20 years ago in 126 recipients, all of whom were under 18 years of age. Eighty-six of these pediatric recipients were treated before 1980 with azathioprine (or eyclophosphamide) and prednisone ...
B.W. Shaw Jr.   +12 more
core   +2 more sources

Plaque‐Like Dermatofibroma: A Case Report and a Review of the Literature With a Focus on Dermoscopy

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Plaque‐like dermatofibroma (PLDF) is a rare clinical variant of dermatofibroma (DF), characterised by flat, infiltrative lesions, often larger than 50 mm in diameter and located on the trunk or lower extremities. A 44‐year‐old male presented to our clinic with a 20 cm brownish plaque with peripheral satellite lesions on the right antecubital ...
Francesco Cavallo   +7 more
wiley   +1 more source

Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis [PDF]

open access: yes, 2001
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of early childhood characterized by nonmalignant accumulation and multivisceral infiltration of activated T lymphocytes and histiocytes (macrophages).
AnnaCarin Samuelsson   +51 more
core   +2 more sources

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