Hereditary sensory and autonomic neuropathies: types II, III, and IV

Author:

Axelrod Felicia B,Gold-von Simson Gabrielle

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Reference63 articles.

1. Axelrod FB: Autonomic and Sensory Disorders. Principles and Practice of Medical Genetics. Volume3. 5th edition. Edited by: Rimoin DL, Connor JM, Pyeritz RE, Korf BR. Edinburgh: Churchill Livingstone; 2007:2802-2816.

2. Dyck P, Ohta M: Neuronal atrophy and degeneration predominantly affecting peripheral sensory neurons. Peripheral Neuropathy. Volume 2. Edited by: Dyck PJ, Thomas PK, Lambert EH. Philadelphia: WB Saunders; 1975:791.

3. Axelrod FB, Pearson J: Congenital sensory neuropathies. Diagnostic distinction from familial dysautonomia. Am J Dis Child. 1984, 138: 947-954.

4. Riley CM, Day RL, Greely DMcL, Langford WS: Central autonomic dysfunction with defective lacrimation. Pediatrics. 1949, 3: 468-477.

5. Bejaoui K, Uchida Y, Yasuda S, Ho M, Nishijima M, Brown RH, Holleran WM, Hanada K: Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis. J Clin Invest. 2002, 110: 1301-1308. 10.1172/JCI200216450.

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