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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1960 1
1963 1
1967 4
1968 6
1969 2
1970 4
1971 1
1972 2
1973 5
1974 3
1975 1
1976 1
1977 6
1978 2
1979 5
1980 3
1981 1
1982 2
1983 5
1984 2
1985 1
1986 3
1987 2
1988 1
1989 5
1990 3
1991 9
1992 5
1993 2
1994 3
1995 4
1996 3
1997 4
1998 8
1999 4
2000 9
2001 2
2002 2
2004 1
2006 1
2020 1
2024 0

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130 results

Results by year

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Page 1
Adrenoleukodystrophy.
Lenard HG. Lenard HG. Neuropediatrics. 1984 Sep;15 Suppl:16-9. doi: 10.1055/s-2008-1052375. Neuropediatrics. 1984. PMID: 6100794
The Floating-Harbor syndrome.
Majewski F, Lenard HG. Majewski F, et al. Among authors: lenard hg. Eur J Pediatr. 1991 Feb;150(4):250-2. doi: 10.1007/BF01955523. Eur J Pediatr. 1991. PMID: 2029915
Cerebellar mutism syndrome.
Janssen G, Messing-Jünger AM, Engelbrecht V, Göbel U, Bock WJ, Lenard HG. Janssen G, et al. Among authors: lenard hg. Klin Padiatr. 1998 Jul-Aug;210(4):243-7. doi: 10.1055/s-2008-1043886. Klin Padiatr. 1998. PMID: 9743960
Dacrystic seizures reconsidered.
Lenard HG. Lenard HG. Neuropediatrics. 1999 Apr;30(2):107-8. doi: 10.1055/s-2007-973472. Neuropediatrics. 1999. PMID: 10401696 No abstract available.
Multiple intracranial juvenile xanthogranulomas. Case report.
Boström J, Janssen G, Messing-Jünger M, Felsberg JU, Neuen-Jacob E, Engelbrecht V, Lenard HG, Bock WJ, Reifenberger G. Boström J, et al. Among authors: lenard hg. J Neurosurg. 2000 Aug;93(2):335-41. doi: 10.3171/jns.2000.93.2.0335. J Neurosurg. 2000. PMID: 10930023 Review.
[Infantile myoclonic encephalopathy].
Förster C, Lenard HG, Pache HD, Versmold H. Förster C, et al. Among authors: lenard hg. Z Kinderheilkd. 1971;111(1):67-82. Z Kinderheilkd. 1971. PMID: 4328905 German. No abstract available.
Clinical and genetic aspects of X-linked adrenoleukodystrophy.
Gärtner J, Braun A, Holzinger A, Roerig P, Lenard HG, Roscher AA. Gärtner J, et al. Among authors: lenard hg. Neuropediatrics. 1998 Feb;29(1):3-13. doi: 10.1055/s-2007-973526. Neuropediatrics. 1998. PMID: 9553942 Review.
Myopathy in Williams-Beuren syndrome.
Voit T, Kramer H, Thomas C, Wechsler W, Reichmann H, Lenard HG. Voit T, et al. Among authors: lenard hg. Eur J Pediatr. 1991 May;150(7):521-6. doi: 10.1007/BF01958438. Eur J Pediatr. 1991. PMID: 1915507
130 results