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Journal Abstract Search
140 related items for PubMed ID: 5001125
1. Centrencephalic myoclonic-astatic petit mal. Clinical and genetic investigation. Doose H, Gerken H, Leonhardt R, Völzke E, Völz C. Neuropadiatrie; 1970 Aug; 2(1):59-78. PubMed ID: 5001125 [No Abstract] [Full Text] [Related]
2. [The myoclonic astatic petit mal. Clinical course of small epileptic seizures in childhood. With an introduction by Prof. Dr. Dietrich Janz]. Kruse R. Monogr Gesamtgeb Neurol Psychiatr; 1968 Aug; 124():1-126. PubMed ID: 4975966 [No Abstract] [Full Text] [Related]
4. [Generalized primary (centrencephalic) petit-mal-seizures during infancy. A clinical and electroencephalographical long-term follow-up study in 11 patients. Centrencephalic myoclonic-astatic petit mal (author's transl)]. Lagenstein I. Nervenarzt; 1978 Oct; 49(10):588-94. PubMed ID: 103008 [No Abstract] [Full Text] [Related]
5. [Electroencephalography in patients with myoclonus epilepsy (Lafora type) and their family members]. Nanba M, Ota T, Fukunaga S. No To Shinkei; 1966 Dec; 18(12):1165-73. PubMed ID: 4961864 [No Abstract] [Full Text] [Related]
6. [Myoclonic-astatic petit mal and its course. A clinical and electroencephalographic study on 95 patients]. Lagenstein I. Fortschr Med; 1980 Apr 17; 98(15):573-9. PubMed ID: 6771197 [No Abstract] [Full Text] [Related]
7. On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type. A clinical and electroencephalographic study of 399 probands. Tsuboi T, Christian W. Humangenetik; 1973 Jul 20; 19(2):155-82. PubMed ID: 4200688 [No Abstract] [Full Text] [Related]
8. [Classification of epilepsy]. Hess R. Schweiz Med Wochenschr; 1984 Dec 15; 114(50):1891-6. PubMed ID: 6440292 [Abstract] [Full Text] [Related]
9. [Centrencephalic myoclonic-astatic petit mal. Clinical and electroencephalographic long-term follow-up study in 52 patients (author's transl)]. Langenstein I. EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1978 Jun 15; 9(2):86-96. PubMed ID: 97076 [Abstract] [Full Text] [Related]
10. Computerized cranial transverse axial tomography (CTAT) in 145 patients with primary and secondary generalized epilepsies. West syndrome, myoclonic-astatic petit mal, absence epilepsy. Lagenstein I, Kühne D, Sternowsky HJ, Rothe M. Neuropadiatrie; 1979 Feb 15; 10(1):15-28. PubMed ID: 107475 [No Abstract] [Full Text] [Related]
11. [Photoconvulsive and photomyoclonic reactions: age-dependent, genetically determined variants of enhanced photosensitivity]. Rabending G, Klepel H. Neuropadiatrie; 1970 Dec 15; 2(2):164-72. PubMed ID: 5001029 [No Abstract] [Full Text] [Related]
12. [The course of myoclonic-astatic petit mal]. Munde B, Todt H. Kinderarztl Prax; 1974 Feb 15; 42(2):60-6. PubMed ID: 4218282 [No Abstract] [Full Text] [Related]
13. Petit mal. Ohtahara S. Dev Med Child Neurol; 1968 Apr 15; 10(2):256. PubMed ID: 4968180 [No Abstract] [Full Text] [Related]
14. Pyknoleptic petit mal. Drury I, Dreifuss FE. Acta Neurol Scand; 1985 Oct 15; 72(4):353-62. PubMed ID: 3936329 [Abstract] [Full Text] [Related]
15. Heredity and generalized epilepsy. Vercelletto P, Courjon J. Epilepsia; 1969 Mar 15; 10(1):7-21. PubMed ID: 4976753 [No Abstract] [Full Text] [Related]
16. [Catamnestic studies in petit mal epilepsy]. Mackiewicz J, Orzechowska-Wolczyk M, Poźniak-Patewicz E, Wendorff J. Neurol Neurochir Pol; 1972 Mar 15; 6(5):749-53. PubMed ID: 4629343 [No Abstract] [Full Text] [Related]
17. [Petit mal state with myoclonic phenomena; 3 electroclinical cases in elderly patients]. Gemignani F, Lechi A, Lisi R, Terzano MG, Mancia D. Riv Neurol; 1978 Mar 15; 48(5):564-74. PubMed ID: 106455 [No Abstract] [Full Text] [Related]
18. Common generalized epilepsy. The so-called idiopathic or centrencephalic epilepsy. Niedermeyer E. Eur Neurol; 1973 Mar 15; 9(3):133-56. PubMed ID: 4632242 [No Abstract] [Full Text] [Related]
19. [Unverricht-Lundborg myoclonic epilepsy in 3 siblings]. Jezierska K, Nawrocka I. Neurol Neurochir Pol; 1971 Mar 15; 5(2):241-4. PubMed ID: 4252636 [No Abstract] [Full Text] [Related]
20. [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 15; 45(11):595-601. PubMed ID: 4217888 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]