Results 31 to 40 of about 5,117,941 (155)

An aberrant bald eagle (Haliaeetus leucocephalus) with multiple anatomical abnormalities

Vertebrate Anatomy, Morphology, Palaeontology, 2019
Genetic abnormalities, especially polydactyly, are quite common among birds. Although there are numerous accounts of anatomically abnormal birds with polydactyly, few written anatomical descriptions have elucidated whether or not these physical ...
Jeremy Klingler, Christine Glasmann
doaj   +3 more sources

Exploring the Impact of Cytogenetic Abnormalities on Treatment Responses and Survival Outcomes in Multiple Myeloma: A Single-Centre Experience of 13 Years of Follow-Up

Biomedicines
(1) Background: The introduction of novel therapies has led to a considerable evolution in the management of Multiple Myeloma, and chromosomal abnormalities predict the success of treatment.
Mehmet Ali Kazgı, Ertugrul Bayram, Tolga Kosecı, Burak Mete, Tugba Toyran, Melek Ergin, Ismail Oguz Kara   +6 more
doaj   +1 more source

Evaluation of mental retardation - Part 1: Etiologic classification of 4659 patients with mental retardation or multiple congenital abnormality and mental retardation

Journal of Pediatric Neurosciences, 2007
Patients with multiple congenital abnormalities and mental retardation are the most frequent patient group who are referred to a genetic clinic. Specific diagnosis for these patients will provide a better understanding of the possible reasons of ...
Adnan Yuksel, Hulya Kayserili, Gozde Yesil, Memnune Yuksel Apak   +3 more
doaj   +1 more source

Colour Vision Abnormalities in Multiple Sclerosis [PDF]

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 1987
ABSTRACT:A battery of colour vision tests was employed to evaluate visual function in patients with multiple sclerosis (M.S.). Colour deficits were found in 45% of patients tested with the Ishihara plates and 42.5% of patients tested with the FM 100-Hue test. 65% of M.S.
A C, Harrison, W J, Becker, W K, Stell
openaire   +2 more sources

Co-Occurrence of Multiple Endocrine Abnormalities Induced by the DIHS/DRESS

International Journal of Endocrinology, 2019
Background. Drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms (DIHS/DRESS) is a severe adverse reaction caused by specific drugs.
Mingqun Deng, Han Wu, Miao Yu, Yi Tian, Yuxiu Li, Xinhua Xiao   +5 more
doaj   +1 more source

Odds ratio of developing neuroimaging abnormalities by 2 categories of serum 25(OH)D concentrations after multiple imputation.

, 2016
Odds ratio of developing neuroimaging abnormalities by 2 categories of serum 25(OH)D concentrations after multiple imputation.
Paulo H. M. Chaves (2742463), Oscar L. Lopez (513426), Katarina Kos (428474), Iain A. Lang (2742457), Lewis H. Kuller (301146), Kenneth M. Langa (570212), Cedric Annweiler (517862), David J. Llewellyn (744962), Bryan R. Kestenbaum (2742466), Olivier Beauchet (517863), William E. Henley (311559), Thomas J. Littlejohns (2742460)   +11 more
core   +1 more source

Odds ratio of developing neuroimaging abnormalities by 3 categories of serum 25(OH)D concentrations after multiple imputation.

, 2016
Odds ratio of developing neuroimaging abnormalities by 3 categories of serum 25(OH)D concentrations after multiple imputation.
Paulo H. M. Chaves (2742463), Oscar L. Lopez (513426), Katarina Kos (428474), Iain A. Lang (2742457), Lewis H. Kuller (301146), Kenneth M. Langa (570212), Cedric Annweiler (517862), David J. Llewellyn (744962), Bryan R. Kestenbaum (2742466), Olivier Beauchet (517863), William E. Henley (311559), Thomas J. Littlejohns (2742460)   +11 more
core   +1 more source

Paracellin-1 gene mutation with multiple congenital abnormalities [PDF]

, 2006
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is an autosomal recessive renal tubular disorder characterized by renal magnesium wasting, hypercalciuria, advanced nephrocalcinosis and progressive renal failure.
Kavukçu, Salih, Böber, Ece, Konrad, Martin, Türkmen, Mehmet, Kasap, Belde, Soylu, Alper   +5 more
core   +2 more sources

Cytogenetic anomalies in Multiple Myeloma patients:A single center study

Genetics & Applications, 2019
Conventional karyotyping in the patients with Multiple myeloma (MM) is very important. Because chromosomal abnormalities which detected in these patients have diagnostic and prognostic value.
Süreyya Bozkurt, Yahya Büyükaşık, Haluk Demiroğlu, Elifcan Aladağ Karakulak, Müfide Okay, Ayşe Karataş, Salih Aksu, İbrahim Haznedaroğlu, Nilgün Sayınalp, Osman Özcebe, Hakan Göker   +10 more
doaj  

Long-term prognostic impact of chromosome 1 abnormalities in newly diagnosed multiple myeloma patients: a monocentric study

Annals of Hematology
The presence of chromosome 1 abnormalities in multiple myeloma (MM) has been included in the more recent prognostic staging system; however, the prognostic role of chromosome 1 abnormalities remains controversial. Thus, in this study we have investigated
Nicolas Thomas Iannozzi, Gabriella Sammarelli, Andrea Poletti, Giannalisa Todaro, Matia Bernardi, Matteo Scita, Anna Benedetta Dalla Palma, Vincenzo Raimondi, Oxana Lungu, Eleonora Carboni, Stefania Ricci, Camilla Sitzia, Mattia Dessena, Rosanna Vescovini, Denise Toscani, Paola Storti, Nicola Giuliani   +16 more
doaj   +1 more source