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From the following article

Anatomy and development and physiology of the larynx

Clarence T. Sasaki

GI Motility online (2006)

doi:10.1038/gimo7

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Figure 1

Structure and function of the larynx viewed phylogenetically (according to Negus)

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Figure 2

The nasolaryngeal relationship.

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Figure 3

Human larynx and pharynx viewed from behind.

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Figure 4

Frontal section through the human larynx demonstrating the valvular structure of the false and true cords.

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Figure 5

Laryngoscopic view of the intrinsic muscles responsible for activating vocal cord position.

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Figure 7

Stimulation of right internal branch of superior laryngeal nerve.

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Figure 8

Intrathoracic pressure is plotted with respect to time (t) in the spontaneously breathing animal.

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Figure 9

Threshold of the adductor reflex is plotted with respect to respiratory phase.

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Figure 10

Threshold of the adductor reflex is plotted with respect to arterial pCO2.

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Figure 11

The increasing pattern of adductor responses (upper) and integrated responses (lower) by 8-Hz stimulation of the superior laryngeal nerve (SLN) (0.6 V, 0.1 msec) under conditions of (a) pCO2 60 mmHg; (b) pCO2 40 mmHg; and (c) pCO2 25 mmHg.

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Figure 12

Threshold of the adductor reflex is plotted with respect to arterial pO2.

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Figure 13

The pattern of adductor responses (upper) and integrated responses (lower) by 8-Hz stimulation of SLN (0.6 V, 0.1 msec) under conditions of (a) pO2 25 mmHg; (b) pO2 100 mmHg; and (c) pO2 150 mmHg.

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Figure 14

Threshold of the adductor reflex is plotted with respect to intrathoracic pressure.

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Figure 15

Influence of body temperature on threshold and latency in (a) 3-week-old puppies; (b) 6-week-old puppies; (c) 12-week-old puppies; (d) adult dogs.

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Figure 16

Influence of body temperature on threshold in four age groups.

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Figure 17

Evoked adductor responses elicited by single-shock stimulation of SLN in (a) 3-week-old puppies; (b) 6-week-old puppies; (c) 12-week-old puppies; (d) adult dogs. S, stimulus artifact.

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Figure 18

Influence of body temperature on latency in four age groups.

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Figure 21

Cricothyroid EMG (upper tracing) and phrenic EMG (lower tracing).

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Figure 22

Glottic alteration produced by cricothyroid (CT) and posterior cricoarytenoid action (PCA) alone and in combination.

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Figure 23

Cricothyroid response to mechanical ventilation at rates of (a) 20 per minute, (b) 30 per minute, (c) 40 per minute.

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Figure 24

Duration of positive pressure stimulation determines duration of cricothyroid-evoked activity.

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Figure 25

a: Vagotomy produces spontaneous inspiratory hyperactivity of cricothyroid motoneurons.

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Figure 26

The threshold of cricothyroid elicitation in response to rate of tracheal pressure change measures 30 cmH2O/sec in normocapnia.

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Figure 27

Thyroarytenoid action potentials elicited by single-shock stimuli applied to the ipsilateral superior laryngeal nerve.

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Figure 28

Thyroarytenoid action potentials elicited by repetitive stimulation of ipsilateral superior laryngeal nerve in control dogs.

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Figure 29

Thyroarytenoid action potentials elicited by superior laryngeal stimulation in tracheostomized dogs.

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Figure 30

Thyroarytenoid action potentials produced by 16-Hz superior laryngeal stimulation in chronically tracheostomized dogs.

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Figure 31

Laryngeal abductor activity 1 week posttracheostomy.

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Figure 32

Laryngeal abductor activity 4 weeks posttracheostomy.

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Figure 33

Placement of pressure transducer.

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Figure 34

Organizational model of the glottic closure reflex pathway demonstrating the effect of a unilateral SLN section.

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Figure 35

Organizational model demonstrating the effect of converting a unilateral recurrent laryngeal nerve (RLN) section (a) to a combined unilateral RLN-superior laryngeal nerve (SLN) section (b) when motor neurons involved ipsilaterally are exceeded by those contralaterally.

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Figure 36

Organizational model demonstrating the effect of converting a unilateral RLN section (a) to a combined unilateral RLN-SLN section (b) when motor neurons involved ipsilaterally are exceeded by those contralaterally.

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Figure 37

Organizational model demonstrating the effect of converting a unilateral RLN section (a) to a combined unilateral RLN-SLN section (b) when motor neurons involved ipsilaterally outnumber those contralaterally.

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Table 1 - Unfortunately we are unable to provide accessible alternative text for this. If you require assistance to access this image, or to obtain a text description, please contact npg@nature.com

Table 1

Sensory innervation of the larynx

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Table 2

Motor innervation of the larynx

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Table 3

Efficiency and latency of responses to stimulation of branches of the superior laryngeal nerves

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Table 4

Effect of core temperature and age on threshold of the adductor reflex in beagles*

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Table 5

Effect of core temperature and age on latency of the adductor reflex in beagles*

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Table 6

Effect of section of different laryngeal nerves on glottic closure force in man (glottic closing force in mmHg)

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Table 7

Percent reduction in glottic closing force by section of different laryngeal nerves*

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