Lenard HG - Search Results

1

Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy.

Herrmann R, Straub V, Blank M, Kutzick C, Franke N, Jacob EN, Lenard HG, Kröger S, Voit T. Herrmann R, et al. Among authors: lenard hg. Hum Mol Genet. 2000 Sep 22;9(15):2335-40. doi: 10.1093/oxfordjournals.hmg.a018926. Hum Mol Genet. 2000. PMID: 11001938

2

Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalism.

Cohn RD, Gillessen-Kaesbach G, Dobyns WB, Kahn T, Lenard HG, Voit T. Cohn RD, et al. Among authors: lenard hg. Am J Med Genet. 1996 May 3;63(1):314-7. doi: 10.1002/(SICI)1096-8628(19960503)63:1<314::AID-AJMG52>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8723127

3

Fetal CNS damage after exposure to maternal trauma during pregnancy.

Baethmann M, Kahn T, Lenard HG, Voit T. Baethmann M, et al. Among authors: lenard hg. Acta Paediatr. 1996 Nov;85(11):1331-8. doi: 10.1111/j.1651-2227.1996.tb13920.x. Acta Paediatr. 1996. PMID: 8955461

4

Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndrome.

Göhlich-Ratmann G, Baethmann M, Lorenz P, Gärtner J, Goebel HH, Engelbrecht V, Christen HJ, Lenard HG, Voit T. Göhlich-Ratmann G, et al. Among authors: lenard hg. Am J Med Genet. 1998 Sep 23;79(3):161-7. doi: 10.1002/(sici)1096-8628(19980923)79:3<161::aid-ajmg2>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9788554

5

Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosis.

Voit T, Krogmann O, Lenard HG, Neuen-Jacob E, Wechsler W, Goebel HH, Rahlf G, Lindinger A, Nienaber C. Voit T, et al. Among authors: lenard hg. Neuropediatrics. 1988 May;19(2):62-71. doi: 10.1055/s-2008-1052404. Neuropediatrics. 1988. PMID: 3374765

6

Pallister-Killian syndrome in older children and adolescents.

Horneff G, Majewski F, Hildebrand B, Voit T, Lenard HG. Horneff G, et al. Among authors: lenard hg. Pediatr Neurol. 1993 Jul-Aug;9(4):312-5. doi: 10.1016/0887-8994(93)90071-j. Pediatr Neurol. 1993. PMID: 8216546

7

Multisystem triglyceride storage disorder without ichthyosis in two siblings.

Wessalowski R, Schroten H, Neuen-Jacob E, Reichmann H, Melnik BC, Lenard HG, Voit T. Wessalowski R, et al. Among authors: lenard hg. Acta Paediatr. 1994 Jan;83(1):93-8. doi: 10.1111/j.1651-2227.1994.tb12960.x. Acta Paediatr. 1994. PMID: 8193482

8

Hearing loss in facioscapulohumeral dystrophy.

Voit T, Lamprecht A, Lenard HG, Goebel HH. Voit T, et al. Among authors: lenard hg. Eur J Pediatr. 1986 Sep;145(4):280-5. doi: 10.1007/BF00439401. Eur J Pediatr. 1986. PMID: 3769995

9

Spontaneous regression of a temporal arachnoid cyst.

Weber R, Voit T, Lumenta C, Lenard HG. Weber R, et al. Among authors: lenard hg. Childs Nerv Syst. 1991 Nov;7(7):414-5. doi: 10.1007/BF00304210. Childs Nerv Syst. 1991. PMID: 1794123

10

Sudden loss of hearing and vestibular function, muscular weakness, and multiple white matter lesions in preschool children.

Lenard HG, Voit T, Lamprecht A, Kahn T, Neuen-Jacob E, Ruitenbeek W. Lenard HG, et al. Neuropediatrics. 1992 Aug;23(4):221-4. doi: 10.1055/s-2008-1071347. Neuropediatrics. 1992. PMID: 1407391

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

126 results

Search Page

Filters