Author/Creator: Hanefeld, F - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Hanefeld, F

1. Congenital adrenal hyperplasia. Report of a case with neurological complications. Issue 7 (July 1973)

Authors:: Hanefeld, F; Crome, L; France, N E; Jackson, A D
Journal:: Archives of disease in childhood
Issue:: Volume 48:Issue 7(1973)
Page Start:: 554
Record Type:: Journal Article
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2. Anoxic ATP depletion in neonatal mice brainstem is prevented by creatine supplementation. Issue 3 (1st May 2000)

Authors:: Wilken, B; Ramirez, J M; Probst, I; Richter, D W; Hanefeld, F
Journal:: Archives of disease in childhood
Issue:: Volume 82:Issue 3(2000)
Page Start:: F224
Record Type:: Journal Article
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3. Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28. Issue 12 (December 1998)

Authors:: Webb, T; Clarke, A; Hanefeld, F; Pereira, J L; Rosenbloom, L; Woods, C G
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 12(1998)
Page Start:: 997
Record Type:: Journal Article
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4. Baló's concentric sclerosis associated with primary human herpesvirus 6 infection. Issue 12 (16th November 2005)

Authors:: Pohl, D; Rostasy, K; Krone, B; Hanefeld, F
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 76:Issue 12(2005)
Page Start:: 1723
Record Type:: Journal Article
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5. MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution. Issue 8 (1st August 2002)

Authors:: Laccone, F; Zoll, B; Huppke, P; Hanefeld, F; Pepinski, W; Trappe, R
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 8(2002)
Page Start:: 586
Record Type:: Journal Article
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6. Identification of a new DMD gene deletion by ectopic transcript analysis. Issue 9 (September 1992)

Authors:: Rininsland, F; Hahn, A; Niemann-Seyde, S; Slomski, R; Hanefeld, F; Reiss, J
Journal:: Journal of medical genetics
Issue:: Volume 29:Issue 9(1992)
Page Start:: 647
Record Type:: Journal Article
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7. Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome. Issue 5 (1st May 2003)

Authors:: Gill, H; Cheadle, J P; Maynard, J; Fleming, N; Whatley, S; Cranston, T; Thompson, E M; Leonard, H; Davis, M; Christodoulou, J; Skjeldal, O; Hanefeld, F; Kerr, A; Tandy, A; Ravine, D; Clarke, A
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 5(2003)
Page Start:: 380
Record Type:: Journal Article
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