nodular sclerosis

Known as: Hodgkin's disease, nodular sclerosis, NSHD, Hodgkin's disease nodular sclerosis NOS 
A subtype of classical Hodgkin lymphoma characterized by collagen bands that surround at least one nodule, and Hodgkin and Reed-Sternberg cells with… (More)
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
PURPOSE Programmed cell death ligand 1 (PD-L1) is an immunomodulatory molecule expressed by antigen-presenting cells and select… (More)
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2013
2013
BACKGROUND Non-syndromic hearing loss (NSHL) is the most common sensory impairment in humans. Until recently its extreme genetic… (More)
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2011
2011
Using data from eight UK cohorts participating in the Healthy Ageing across the Life Course (HALCyon) research programme, with… (More)
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Highly Cited
2010
Highly Cited
2010
The extreme genetic heterogeneity of nonsyndromic hearing loss (NSHL) makes genetic diagnosis expensive and time consuming using… (More)
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Highly Cited
2009
Highly Cited
2009
A20 is a negative regulator of the NF-κB pathway and was initially identified as being rapidly induced after tumour-necrosis… (More)
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Highly Cited
2003
Highly Cited
2003
Mediastinal large B-cell lymphoma (MLBCL) is a recently identified subtype of diffuse large B-cell lymphoma (DLBCL) that… (More)
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Highly Cited
2002
Highly Cited
2002
Congenital profound deafness has a known genetic origin in more than 50% of all cases. The majority of the non syndromic hearing… (More)
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Highly Cited
2000
Highly Cited
2000
OBJECTIVE Mutations in the GJB2 gene are a major cause of autosomal recessive and sporadic types of congenital deafness. The… (More)
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Highly Cited
2000
Highly Cited
2000
Although eosinophilic granulocytes are frequently observed in lymphatic tissue of Hodgkin's patients, no substantial data reveal… (More)
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Highly Cited
1966
Highly Cited
1966
into the following 6 groups: (a) lymphocytic and/or histiocytic (L & H),1 nodular; (b) lymphocytic and/or histiocytic (L & H… (More)
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