The American anatomical memoirs / Wistar Institute of Anatomy and Biology.

no. 17 (1939)

The American anatomical memoirs / Wistar Institute of Anatomy and Biology.

no. 15 (1929)

The American anatomical memoirs / Wistar Institute of Anatomy and Biology.

no. 14 (1929)

The American anatomical memoirs / Wistar Institute of Anatomy and Biology.

no. 16 (1938)

The American anatomical memoirs / Wistar Institute of Anatomy and Biology.

no. 18 (1939)

The American anatomical memoirs / Wistar Institute of Anatomy and Biology.

no. 20 (1942)

The genus Bostryx in central western Argentina: anatomical and distributional description of four of its southernmost species (Gastropoda, Bulimulidae)

ABSTRACT The genus Bostryx Troschel, 1847 is endemic to South America, extending from Ecuador to Chile and Argentina. The southernmost Argentinian species of the genus that inhabit San Luis, San Juan and Mendoza provinces, specially the pre-Andes, Andes and Sierras Pampeanas mountain ranges, were examined. This is the first time the anatomy of Bostryx pastorei (Holmberg, 1912), Bostryx reedi (Parodiz, 1947) and Bostryx strobeli (Parodiz, 1956) has been described.Bostryx cordillerae (Strobel, 1874) is re-described regarding shell and anatomy due to new morphological data. The main differences among the species examined are based on shell characters. The distribution ofBostryx mendozanus (Strobel, 1874) and Bostryx cuyanus (Pfeiffer, 1867), other species found in this region, was also discussed.

The microscope and histology for the use of laboratory students in the anatomical department of Cornell University. by Simon Henry Gage.

3rd ed

Anatomical landmarks for transnasal endoscopic skull base surgery.

Resection of midline skull base lesions involve approaches needing extensive neurovascular manipulation. Transnasal endoscopic approach (TEA) is minimally invasive and ideal for certain selected lesions of the anterior skull base. A thorough knowledge of endonasal endoscopic anatomy is essential to be well versed with its surgical applications and this is possible only by dedicated cadaveric dissections. The goal in this study was to understand endoscopic anatomy of the orbital apex, petrous apex and the pterygopalatine fossa. Six cadaveric heads (3 injected and 3 non injected) and 12 sides, were dissected using a TEA outlining systematically, the steps of surgical dissection and the landmarks encountered. Dissection done by the "2 nostril, 4 hands" technique, allows better transnasal instrumentation with two surgeons working in unison with each other. The main surgical landmarks for the orbital apex are the carotid artery protuberance in the lateral sphenoid wall, optic nerve canal, lateral optico-carotid recess, optic strut and the V2 nerve. Orbital apex includes structures passing through the superior and inferior orbital fissure and the optic nerve canal. Vidian nerve canal and the V2 are important landmarks for the petrous apex. Identification of the sphenopalatine artery, V2 and foramen rotundum are important during dissection of the pterygopalatine fossa. In conclusion, the major potential advantage of TEA to the skull base is that it provides a direct anatomical route to the lesion without traversing any major neurovascular structures, as against the open transcranial approaches which involve more neurovascular manipulation and brain retraction. Obviously, these approaches require close cooperation and collaboration between otorhinolaryngologists and neurosurgeons.

Getting in touch: segregated somatosensory what and where pathways in humans revealed by electrical neuroimaging.

Whether the somatosensory system, like its visual and auditory counterparts, is comprised of parallel functional pathways for processing identity and spatial attributes (so-called what and where pathways, respectively) has hitherto been studied in humans using neuropsychological and hemodynamic methods. Here, electrical neuroimaging of somatosensory evoked potentials (SEPs) identified the spatio-temporal mechanisms subserving vibrotactile processing during two types of blocks of trials. What blocks varied stimuli in their frequency (22.5 Hz vs. 110 Hz) independently of their location (left vs. right hand). Where blocks varied the same stimuli in their location independently of their frequency. In this way, there was a 2x2 within-subjects factorial design, counterbalancing the hand stimulated (left/right) and trial type (what/where). Responses to physically identical somatosensory stimuli differed within 200 ms post-stimulus onset, which is within the same timeframe we previously identified for audition (De Santis, L., Clarke, S., Murray, M.M., 2007. Automatic and intrinsic auditory "what" and "where" processing in humans revealed by electrical neuroimaging. Cereb Cortex 17, 9-17.). Initially (100-147 ms), responses to each hand were stronger to the what than where condition in a statistically indistinguishable network within the hemisphere contralateral to the stimulated hand, arguing against hemispheric specialization as the principal basis for somatosensory what and where pathways. Later (149-189 ms) responses differed topographically, indicative of the engagement of distinct configurations of brain networks. A common topography described responses to the where condition irrespective of the hand stimulated. By contrast, different topographies accounted for the what condition and also as a function of the hand stimulated. Parallel, functionally specialized pathways are observed across sensory systems and may be indicative of a computationally advantageous organization for processing spatial and identity information.