Results 31 to 40 of about 5,676,953 (305)

Neu Laxova syndrome

Indian Journal of Pathology and Microbiology, 2019
NeuLaxova syndrome (NLS) is a rare congenital abnormality involving multiple systems. Until date, only 60 cases of this syndrome have been reported in the literature.
Tanima Dwivedi, Manasi Gosavi
doaj   +1 more source

The incidence and interrelationship of hemivertebra and concomitant cardiac abnormalities in congenital scoliosis

BMC Musculoskeletal Disorders, 2023
Background Congenital scoliosis(CS) is associated with multiple organs defect, and cardiac abnormalities have been reported commonly associated with CS. Hemivertebra is caused by the failure of vertebral formation, which is a major constitute of CS. Till
Shengru Wang, Yiwei Zhao, You Du, Jianguo Zhang, Bin Yu   +4 more
doaj   +1 more source

Experience of Identity Change in People Who Reported a Diagnosis of Multiple Sclerosis : A Qualitative Inquiry [PDF]

, 2019
Background: A diagnosis of multiple sclerosis (MS) can lead to changes to a person’s sense of self. The aim of this study was to investigate the subjective experience of identity change and subsequent adjustment to MS.
das Nair, Roshan, Smale, Kathryn, Lincoln, NB, Lincoln, Nadina B., Barker, AB, Hunt, N, Smale, K., das Nair, R, Hunt, Nigel, Barker, Alexander B., Barker, A., Smale, K, Lincoln, N.B., Hunt, N.   +13 more
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Peripheral nervous system electrodiagnostic abnormalities in predominantly Hispanic Multiple Sclerosis patients

, 2021
•The prevalence of electrodiagnostic abnormalities, especially axonal polyneuropathy, in the MS population may be higher than previously considered.•The presence of a peripheral axonal polyneuropathy may be important in the context of central axonopathy ...
Weinstock-Guttman, Bianca, Alexis A Lizarraga, Bianca Weinstock-Guttman, Rammohan, Kottil W, Sharma, Khema, Khema Sharma, Kottil W Rammohan, Lizarraga, Alexis A   +7 more
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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
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Diffusion imaging shows abnormalities after blunt head trauma when conventional magnetic resonance imaging is normal [PDF]

, 2001
The investigation and management of patients after head injury must include the accurate and complete identification of cerebral damage. Using diffusion tensor imaging, abnormalities of diffusion in patients with head injuries and unremarkable MRI have ...
F J Rugg-Gunn, DUNCAN, JS, Duncan, J.S., SYMMS, MR, RUGG-GUNN, FJ, Barker, Gareth; id_orcid, GREENWOOD, R, Barker, G.J., Greenwood, R., Symms, M.J., Rugg-Gunn, F.J.   +10 more
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T2 lesion location really matters: a 10 year follow-up study in primary progressive multiple sclerosis [PDF]

, 2010
Objectives: Prediction of long term clinical outcome in patients with primary progressive multiple sclerosis (PPMS) using imaging has important clinical implications, but remains challenging.
Polman, C., Barkhof, F., Montalban, X, CHARD D, Thompson, A, Polman, C, F. Barkhof, Chard, D, Samson, R., D. Miller, Bodini, B., A. Thompson, Samson, R, MONTALBAN X, R. Samson, Rovira, A, POLMAN C, KHALEELI Z, O. Ciccarelli, Filippi, M., N. De Stefano, Barkhof, F, BATTAGLINI, MARCO, B. Bodini, A. Rovira, Battaglini, M, Polman, C.H., Chard, D., CICCARELLI O., Miller, D., Rovaris, M, Battaglini, M., Thompson, A., De Stefano, N., X. Montalban, MILLER D, ROVARIS M, FILIPPI M, D. Chard, Khaleeli, Z, SAMSON R, ROVIRA A, THOMPSON A, Rovaris, M., De Stefano, N, Rovira, A., Z. Khaleeli, Bodini, B, BODINI B, M. Filippi, Miller, D, BARKHOF F, DE STEFANO, NICOLA, M. Rovaris, Montalban, X., Ciccarelli, O., Ciccarelli, O, Khaleeli, Z., M. Battaglini, C. Polman, Filippi, M, Rovira, Alex, Stefano, N. De, Rovaris, Marco, Thompson, Alan, De Stefano N, Battaglini M, FILIPPI , MASSIMO, Barkhof, Frederik, Polman, Chris, Montalban, Xavier, Ciccarelli, Olga, Miller, David, Filippi, Massimo, Khaleeli, Zhaleh, Chard, Declan, Filippi, M., Bodini, Benedetta, Samson, Rebecca   +78 more
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Clinical Significance of TP53 Abnormalities in Newly Diagnosed Multiple Myeloma

Turkish Journal of Hematology, 2021
Objective: This study aimed to identify the clinical significance of TP53 and common cytogenetic abnormalities. Materials and Methods: A total of 114 patients with newly diagnosed multiple myeloma (MM) and TP53 abnormalities were selected from two large ...
Fang Ye, Tongtong Wang, Aijun Liu, Yanchen Li, Ningning Li, Huan Wang, Wenming Chen   +6 more
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Grey matter alterations co-localize with functional abnormalities in developmental dyslexia : an ALE meta-analysis [PDF]

, 2012
The neural correlates of developmental dyslexia have been investigated intensively over the last two decades and reliable evidence for a dysfunction of left-hemispheric reading systems in dyslexic readers has been found in functional neuroimaging studies.
Lonnemann, Jan, Fiebach, Christian, Fiebach Christian J., Jan Lonnemann (141630), Sven Lindberg (141631), Lindberg Sven, Marcus Hasselhorn (141633), Christian J Fiebach, Janosch Linkersdörfer (141629), Christian J. Fiebach (141636), Lindberg, S., Sven Lindberg, Linkersdörfer, Janosch, Marcus Hasselhorn, Lonnemann Jan, Fiebach, C.J., Linkersdörfer Janosch, Lindberg, Sven, Hasselhorn Marcus, Jan Lonnemann, Linkersdörfer, J., Hasselhorn, M., Hasselhorn, Marcus, Lonnemann, J., Janosch Linkersdörfer   +24 more
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Toxocara infection in the differential diagnosis of multiple sclerosis in the Middle East [PDF]

, 2020
A critical step in the diagnosis of multiple sclerosis is to rule out a heterogeneous variety of multiple sclerosis mimickers, which is crucial in the era of powerful immune-modulator treatments.
El Najjar, Mayssam, El-Ayoubi, Nabil K., Atweh, Samir F., Baalbaki, Marwa M.   +3 more
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