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Biologie Quiz am Neurodeg3AD, erstellt von Mak Sch am 30/11/2017.

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Neurodeg3AD

Frage 1 von 12

1

Cognitive features impaired in AD are:

Wähle eine der folgenden:

  • Attentional and executive deficits

  • Anterograde episodic memory

  • Semantics

  • All of the above

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Frage 2 von 12

1

Question 2
Working memory is:
(multiple answers are possible)

Wähle eine oder mehr der folgenden:

  • A. a cognitive system that is responsible for the transient holding, processing, and manipulation of information

  • B. an executive controller that interacts with separate short-term stores for auditory-verbal and visuo-spatial information

  • C. a cognitive system where information can be stored for long periods of time

  • D. a limited capacity system that is capable of briefly storing and manage information involved in the performance of complex cognitive tasks such as reasoning, comprehension and certain types of learning

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Frage 3 von 12

1

Synaptic loss is a prominent early pathological feature of AD, and closely associated to cognitive decline, it is mainly localized:
Answers:

Wähle eine der folgenden:

  • A. Hippocampus

  • B. Diffuse in all the brain

  • C. Mainly in Cortices

  • D. Entorhinal cortex

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Frage 4 von 12

1

Described by Braak and Braak, tangles sequentially appear in the following specific regions as AD progresses:

Wähle eine oder mehr der folgenden:

  • A. Limbic-Isocortical-Transentorihnal

  • B. Transetorihnal-Limbic-Isocortical

  • C. Isocortical-Transentorihnal- Limbic

  • D. Transentorihnal- Isocortical-Limbic

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Frage 5 von 12

1

In Anterograde Amnesia: (multiple answers possible)
Answers:


Wähle eine oder mehr der folgenden:

  • A. Memories created prior to the event that caused the amnesia are lost while new memories can still be created.

  • B. There is loss of the ability to create new memories after the event that caused the amnesia, leading to a partial or complete inability to recall the recent past

  • C. New memories can still be created.

  • D. Long-term memories from before the event remain intact

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Frage 6 von 12

1

Question 6
One of the earliest pathological changes on AD is the increase in tangle Tau formation in:

Wähle eine der folgenden:

  • A. Transenthorhinal region

  • B. Striatum

  • D. Parietal cortex

  • C. Prefrontal cortex

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Frage 7 von 12

1

The most common familial early onset AD is related to:



Wähle eine oder mehr der folgenden:

  • A. Presenilin 2 gene at Chromosome 1

  • B. Apolipoprotein E gene at Chromosome 19

  • C. Presenilin 1 gene at Chromosome 14

  • D. Amyloid protein precursor at Chromosome 21

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Frage 8 von 12

1

Question 8
Studies of AD patients with FDG-PET + MRI coregistration (Positron emission tomography with fluoro-2-deoxy-D-glucose in combination to Magnetic Resonance Imaging) revealed the importance of the following structures in the site of early pathology in AD
(multiple answers possible)

Wähle eine oder mehr der folgenden:

  • A. Posterior cingulate

  • D. Mediotemporal lobe

  • C. Mammillary bodies and thalamus,

  • B. Retrosplenial cortex

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Frage 9 von 12

1

Question 9
Other early pathological changes on AD is the increase in amyloid plaques in:
(multiple answer possible)

Wähle eine oder mehr der folgenden:

  • A. Transenthorhinal region

  • D. Parietal cortex

  • B. Posterior cinguate cortex

  • C. Frontal and association cortices

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Frage 10 von 12

1

Question 10
The greatest risk factors for Alzheimer's are: (multiple answers possible)

Wähle eine oder mehr der folgenden:

  • A. Gender

  • B. Age

  • C. Genetics

  • D. Head injury

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Frage 11 von 12

1

Hallmarks of Alzheimer's include: (multiple answer possible)

Wähle eine oder mehr der folgenden:

  • A. Degeneration of hippocampal and cortical neurons

  • B. Reduced cholinergic transmission

  • C. Neuritic plaques

  • D. Neurofibrillary Tangles

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Frage 12 von 12

1

The following are the aims of AD treatment active and possible at the present time:
(multiple answers possible)

Wähle eine oder mehr der folgenden:

  • A. Neuroregeneration (reversal of symptomatic decline)

  • B. Augmentation (delay of symptomatic decline)

  • C. Neuroprotection (slowing of symptomatic decline)

  • D. Suppression (inhibition of symptomatic decline)

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