First descriptions of copepodid stages, sexual dimorphism and intraspecific variability of Mesocletodes Sars, 1909 (Copepoda, Harpacticoida, Argestidae), including the description of a new species with broad abyssal distribution [PDF]
, 2011 Mesocletodes Sars, 1909a encompasses 37 species to date. Initial evidence on intraspecific variability and sexual dimorphism has been verified for 77 specimens of Mesocletodes elmari sp. n. from various deep-sea regions, and ontogenetic development has
Menzel, Lena
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The Deer Flies of Indiana (Diptera: Tabanidae: \u3ci\u3eChrysops\u3c/i\u3e) [PDF]
, 2017 (excerpt) The great majority of specimens, over 12,000 out of 13,185, which form the basis of this study, were collected by the writer during the flight season of the summer of 1963.
Burton, John J.S
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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 +6 more
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Hyaline fibromatosis syndrome: cutaneous manifestations [PDF]
Anais Brasileiros de Dermatologia, 2016 Hyaline fibromatosis syndrome is the current name for clinical manifestations of diseases previously known as “infantile systemic hyalinosis” and “juvenile hyaline fibromatosis”.
Silvio Alencar Marques +5 more
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Ultrasound in the diagnosis of calcium pyrophosphate dihydrate deposition disease. A systematic literature review and a meta-analysis [PDF]
, 2016 ..
Adinolfi, A. +11 more
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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 +7 more
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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 +6 more
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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 +3 more
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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
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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 +3 more
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