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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
115 related items for PubMed ID: 3504252
1. What is it? Case 2, 1986. Mov Disord; 1986; 1(4):281-7. PubMed ID: 3504252 [No Abstract] [Full Text] [Related]
11. [Progressive myoclonus epilepsy in two siblings and 5 cases with dyssynergia cerebellaris myoclonica in several generations of a kinship, a clinical and genetic study]. Diebold K, Kastner M, Penin H. Nervenarzt; 1974 Nov 18; 45(11):595-601. PubMed ID: 4217888 [No Abstract] [Full Text] [Related]
14. [Ramsay Hunt syndrome-like symptom complex associated with isolated ACTH deficiency; a case report (author's transl)]. Sasaki H, Ozaki Y, Ohgoshi N, Kanazawa I, Nakanishi T. Rinsho Shinkeigaku; 1982 Jan 18; 22(1):66-73. PubMed ID: 6284428 [No Abstract] [Full Text] [Related]
15. Ramsay Hunt syndrome: to bury or to praise. Berkovic SF, Andermann F. J Neurol Neurosurg Psychiatry; 1990 Jan 18; 53(1):89-90. PubMed ID: 2106013 [No Abstract] [Full Text] [Related]
17. [Biotinidase deficiency. Its form of presentation and response to treatment]. Campistol J, Vilaseca MA, Ribes A, Riudor E. An Esp Pediatr; 1996 Apr 18; 44(4):389-92. PubMed ID: 8796946 [No Abstract] [Full Text] [Related]