Results 31 to 40 of about 121,343 (310)

Ultrasound in the diagnosis of calcium pyrophosphate dihydrate deposition disease. A systematic literature review and a meta-analysis [PDF]

, 2016
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Adinolfi, A., Bertoldi, I., Cimmino, M. A., Delle Sedie, A., Di Sabatino, V., Filippou, G, Filippucci, E., Frediani, B., Iagnocco, Annamaria, Picerno, V., Scirè, C. A., Sconfienza, L. M.   +11 more
core   +3 more sources

Juvenile Hyaline Fibromatosis - Child with Scalp Swellings [PDF]

Journal of Liaquat National Hospital
Juvenile hyaline fibromatosis is a recessive autosomal hereditary disorder characterized by abnormal growth of hyalinized fibrous tissue. Its clinical presentation is manifested by benign skin lesions, bone lesions, joint contractures, and gingival ...
Naila Parveen, Javeria Mansoor, Komal Masroor   +2 more
doaj   +1 more source

Myeloid p38 activation maintains macrophage–liver crosstalk and BAT thermogenesis through IL‐12–FGF21 axis

Hepatology, EarlyView., 2022
Physiological activation of myeloid p38 controls macrophage IL‐12 production and crosstalk to the liver by modulating hepatic FGF21, and subsequently, brown adipose tissue thermogenesis during obesity Abstract Obesity features excessive fat accumulation in several body tissues and induces a state of chronic low‐grade inflammation that contributes to ...
María Crespo, Ivana Nikolic, Alfonso Mora, Elena Rodríguez, Luis Leiva‐Vega, Aránzazu Pintor‐Chocano, Daniel Horrillo, Lourdes Hernández‐Cosido, Jorge L. Torres, Eva Novoa, Rubén Nogueiras, Gema Medina‐Gómez, Miguel Marcos, Magdalena Leiva, Guadalupe Sabio   +14 more
wiley   +1 more source

Juvenile hyaline fibromatosis or infantile systemic hyalinosis: Hyaline fibromatosis syndrome

Indian Journal of Paediatric Dermatology, 2016
Juvenile hyaline fibromatosis or infantile systemic hyalinosis is a rare progressive, fatal autosomal recessive disorder characterized by widespread deposition of hyaline.
K Amrutha Varshini, K Haritha, Chirag A Desai, G Raghurama Rao, A Prasad Chowdary, A Amareswar, P Ramana Murty   +6 more
doaj   +1 more source

Five new coexisting species of copepod crustaceans of the genus Spaniomolgus (Poecilostomatoida: Rhynchomolgidae), symbionts of the stony coral Stylophorapistillata (Scleractinia) [PDF]

, 2018
Spaniomolgus is a symbiotic genus of copepods of the poecilostomatoid family Rhynchomolgidae and is known to be associated with shallow-water reef-building hermatypic corals.
Bandera García, María Eugenia, Conradi Barrena, Mercedes, Ivanenko, Viatcheslav N., Mudrova, Sofya V.   +3 more
core   +2 more sources

Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation

Molecular Genetics & Genomic Medicine, 2020
Background Hyaline fibromatosis syndrome is an autosomal recessive disease caused by mutations in ANTXR2 which leads to loss of function of the transmembrane protein anthrax toxin receptor 2.
Bettina Härter, Francesco Benedicenti, Daniela Karall, Ekkehard Lausch, Gisela Schweigmann, Franco Stanzial, Andrea Superti‐Furga, Sabine Scholl‐Bürgi   +7 more
doaj   +1 more source

Histomorphologic Spectrum in Hyaline Vascular Variant of Castleman Disease [PDF]

Journal of Clinical and Diagnostic Research, 2017
Introduction: Castleman Disease (CD) is a rare lymphoproliferative disorder with heterogenous clinical and pathological features. It is a rare disease with mention in the rare disease data of the orphanet.
Chaithra Gowthuvalli Venkataramana, Hema Kini, Debarshi Saha, Sharada Rai, Deepa Sowkur Anandarama Adiga, Ranjitha Rao, Cheryl Sarah Philipose   +6 more
doaj   +1 more source

Insight into the Taxonomic Resolution of the Pleosporalean Species Associated with Dead Woody Litter in Natural Forests from Yunnan, China

Journal of Fungi, 2022
In the course of investigating the systematics of woody litter micromycete associates in Yunnan Province, China, we found one new species in Phaeoseptaceae, one new genus and three new species in Sulcatisporaceae from 16 specimens collected (ten ...
Dhanushka N. Wanasinghe, Guang-Cong Ren, Jian-Chu Xu, Ratchadawan Cheewangkoon, Peter E. Mortimer   +4 more
doaj   +1 more source

Recurrence in unicentric castleman’s disease postoperatively: a case report and literature review

BMC Surgery, 2018
Background Our case describe a rare recurrence case of Unicentric Castleman’s disease (UCD) with hyaline vascular type 14 years after surgery. Case presentation A 35-year-old Chinese female was admitted to hospital with one and half months history chest ...
Na Ren, Lei Ding, Erna Jia, Jinru Xue
doaj   +1 more source

Comprehensive Cytomorphologic Analysis of Pulmonary Adenoid Cystic Carcinoma: Comparison to Small Cell Carcinoma and Non-pulmonary Adenoid Cystic Carcinoma [PDF]

Journal of Pathology and Translational Medicine, 2015
Background: Cytologic diagnosis of pulmonary adenoid cystic carcinoma (AdCC) is frequently challenging and differential diagnosis with small cell carcinoma is often difficult. Methods: Eleven cytologically diagnosed cases of pulmonary AdCC were collected
Seokhwi Kim, Jinah Chu, Hojoong Kim, Joungho Han   +3 more
doaj   +1 more source