Πλοήγηση ανά Θέμα "DISORDER"

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Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations

Nishino, I.; Spinazzola, A.; Papadimitriou, A.; Hammans, S.; Steiner, I.; Hahn, C. D.; Connolly, A. M.; Verloes, A.; Guimaraes, J.; Maillard, I.; Hamano, H.; Donati, M. A.; Semrad, C. E.; Russell, J. A.; Andreu, A. L.; Hadjigeorgiou, G. M.; Vu, T. H.; Tadesse, S.; Nygaard, T. G.; Nonaka, I.; Hirano, I.; Bonilla, E.; Rowland, L. P.; DiMauro, S.; Hirano, M. (2000)

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal recessive disorder defined clinically by severe gastrointestinal dysmotility; cachexia; ptosis, ophthalmoparesis, or both; peripheral neuropathy; ...
The MoCA Well-suited screen for cognitive impairment in Parkinson disease

Dalrymple-Alford, J. C.; MacAskill, M. R.; Nakas, C. T.; Livingston, L.; Graham, C.; Crucian, G. P.; Melzer, T. R.; Kirwan, J.; Keenan, R.; Wells, S.; Porter, R. J.; Watts, R.; Anderson, T. J. (2010)

Objective: To establish the diagnostic accuracy of the Montreal Cognitive Assessment (MoCA) when screening externally validated cognition in Parkinson disease (PD), by comparison with a PD-focused test (Scales for Outcomes ...
Prevalence of thrombophilic mutations in patients with unprovoked thromboembolic disease. A comparative analysis regarding arterial and venous disease

Mandala, E.; Lafaras, C.; Tsioni, C.; Speletas, M.; Papageorgiou, A.; Kleta, D.; Dardavessis, T.; Ilonidis, G. (2012)

Background: Thromboembolic disease (TED) represents one of the main reasons of morbitity and mortality in Western World. Venous and arterial thrombotic disorders have long been viewed as separate pathophysiological entities. ...
Serotonin and Neuron-specific Enolase: Serum Acute and Mid-term Levels and their Association With Posttraumatic Depression

Wozniak, G.; Georgoulias, P.; Iliadis, C.; Valotasiou, V.; Papadopoulos, G.; Bagiatis, V.; Tsougos, I.; Paterakis, K. N.; Fountas, K. N. (2010)

Objectives: To investigate the association between serotonin (SER), cholesterol, and neuron-specific enolase (NSE) serum levels with depression after traumatic brain injury (TBI). Materials and Methods: Seventy-four patients ...
TEACHER BIASES IN THE IDENTIFICATION OF LEARNING DISABILITIES: AN APPLICATION OF THE LOGISTIC MULTILEVEL MODEL

Sideridis, G. D.; Antoniou, F.; Padeliadu, S. (2008)

The purpose of the present study was to investigate the presence of teacher biases with regard to identification of students with learning disabilities (LD). Factors related to teachers' gender, age, and experience, along ...

Πλοήγηση ανά Θέμα "DISORDER"

Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations ﻿

The MoCA Well-suited screen for cognitive impairment in Parkinson disease ﻿

Prevalence of thrombophilic mutations in patients with unprovoked thromboembolic disease. A comparative analysis regarding arterial and venous disease ﻿

Serotonin and Neuron-specific Enolase: Serum Acute and Mid-term Levels and their Association With Posttraumatic Depression ﻿

TEACHER BIASES IN THE IDENTIFICATION OF LEARNING DISABILITIES: AN APPLICATION OF THE LOGISTIC MULTILEVEL MODEL ﻿

Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations

The MoCA Well-suited screen for cognitive impairment in Parkinson disease

Prevalence of thrombophilic mutations in patients with unprovoked thromboembolic disease. A comparative analysis regarding arterial and venous disease

Serotonin and Neuron-specific Enolase: Serum Acute and Mid-term Levels and their Association With Posttraumatic Depression

TEACHER BIASES IN THE IDENTIFICATION OF LEARNING DISABILITIES: AN APPLICATION OF THE LOGISTIC MULTILEVEL MODEL