| Bogros, Antoine | <person> 19th century French anatomist. See: Bogros' serous membrane. (05 Mar 2000) |
|---|---|
| Ranvier, Louise Antoine | <person> Was a Physician and Histologist. Professor in the College of France, Paris. Ranvier's Nodes - short specialised interruptions in the myelin sheath occurring along myelinated nerve fibres. Responsible for saltatory conduction. Lived: 1835-1922. B. Lyons, 1835, d. 1922. (05 Dec 1998) |
| Marfan, Antoine Bernard-Jean | <person> French paediatrician, 1858-1942. See: Marfan's disease, Marfan's law, Marfan's syndrome. (05 Mar 2000) |
| Petit, Antoine | <person> French surgeon and anatomist, 1718-1794. See: Petit's ligament. (05 Mar 2000) |
| Rouget, Antoine | <person> 19th century French physiologist. See: Rouget's bulb. (05 Mar 2000) |
| Jobert de Lamballe, Antoine | <person> French surgeon, 1799-1867. See: Jobert de Lamballe's fossa, Jobert de Lamballe's suture. (05 Mar 2000) |
| Ferrein, Antoine | <person> French anatomist, 1693-1769. See: Ferrein's canal, Ferrein's cords, Ferrein's foramen, Ferrein's ligament, Ferrein's pyramid, Ferrein's tube, Ferrein's vasa aberrantia, processus ferreini. (05 Mar 2000) |
| Lembert, Antoine | <person> French surgeon, 1802-1851. See: Lembert suture, Czerny-Lembert suture. (05 Mar 2000) |
| Acosta, Joseph de | <person> Spanish Jesuit missionary, 1539-1600. See: Acosta's disease. (05 Mar 2000) |
| Arneth, Joseph | <person> German physician, 1873-1955. See: Arneth classification, Arneth count, Arneth formula, Arneth index, Arneth stages. (05 Mar 2000) |
| Aub, Joseph | <person> U.S. Physician, 1890-1973. See: Aub-DuBois table. (05 Mar 2000) |
| Babinski, Joseph | <person> French neurologist, 1857-1932. See: Babinski's phenomenon, Babinski's sign, Babinski reflex, Babinski's syndrome. (05 Mar 2000) |
| Beau, Joseph | <person> French physician, 1806-1865. See: Beau's lines. (05 Mar 2000) |
| Bertin, Exupere Joseph | <person> French anatomist, 1712-1781. See: Bertin's bones, Bertin's columns, Bertin's ligament, Bertin's ossicles. (05 Mar 2000) |
| Machado-Joseph | A rare form of hereditary ataxia, characterised by onset in early adult life of progressive, spinocerebellar and extrapyramidal disease with external ophthalmoplegia, rigidity dystonia symptoms, and, often, peripheral amyotrophy; found predominantly in people of Azorean ancestry; autosomal dominant inheritance. Synonym: Azorean disease, Portuguese-Azorean disease. Origin: Surnames of two families studied in major descriptions of the disease. (05 Mar 2000) |