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Biomedical subjects

G Boudin

Publications and source records attributed to G Boudin.

At least 19 recordsLinked to original sources
PubMed1985

[Endotracheal tube for laryngeal CO2 laser microsurgery. 208 cases].

To suppress the risk inherent in laryngeal microsurgery performed with a CO2 laser beam, the authors suggest to use a reinforced silicone endotracheal tube, the cuff of which is protected by a silicone plus aluminium powder shield. The resistance of silicone to fire is augmented during laser shots by a nitrogen flow on the upper side of the shield at the rates of 2 l/min in patients breathing air and 30 l/min in patients give oxygen.

Adolescent↗
PubMed1979

[Mesoscopic anatomy of the peribuccal facial muscles].

In 16 human face dissections under the operative microscope, the authors recall the classical anatomy of perioral muscles. Instead of the 3 muscles around the nostrils, they prefer to discern two layers: deep and superficial. The subnasal region can similarly be dissociated. Resuming the commissural node study they insist upon the peculiar role of the platysma muscle and its expansions, and upon the tight imbrication of buccinator and orbicularis oris muscles.

Cheek↗
PubMed1979

[Functional anatomy of the pisiform bone].

The pisiform is the only moving structure of the canalis carpi. In the power grip, it undergoes a posterior and medial movement, limited by the pisohamate ligament. This motion is indispensable for a good prehension. The strength of the pisohamate ligament effectively balances the dislocation tendency the flexors carpi ulnaris exert on the pisiform.

Biomechanical Phenomena↗
PubMed1976

Fatal systemic carnitine deficiency with lipid storage in skeletal muscle, heart, liver and kidney.

A fatal case of systemic carnitine deficiency is reported. The patient suffered from slowly progressive muscle weakness since early childhood. After the age of 17 years her weakness progressed more rapidly until her death at the age of 20. A pregnancy during the last year of the patient's life was followed by rapid deterioration in her condition. An episode of renal insufficiency occurred at the age of 17 years and hepatomegaly, increased BSP dye retention and intermittent ketoacidosis were present during the last month of her life. Biopsy and autopsy specimens of muscle showed a lipid storage myopathy. Type 1 fibers were selectively severely affected, and many Type 1 fibers were atrophic. Abundant large mitochondria, some also containing abnormal inclusions, were also present in the muscle fibers. At autopsy there was marked accumulation of sudanophilic lipid deposits in all hepatocytes, in the renal tubular epithelial cells, and a patchy increase of lipid material was found in the myocardial fibers. There was marked carnitine deficiency in the patient's liver as well as muscel, while the carnitine palmityltransferase activities in these tissues were abnormally high. The basic metabolic abnormality is assumed to be a defect in carnitine biosynthesis.

Adult↗