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1
Oligodendroglioma: incidence and biological behavior in a defined population
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Artigo
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Oligodendroglioma: incidence and biological behavior in a defined population

MØRK, S. J ; LINDEGAARD, K.-E ; HALVORSEN, T. B ; LEHMANN, E. H ; SOLGAARD, T ; HATLEVOLL, R ; HARVEI, S ; GANZ, J

Journal of neurosurgery, 1985-12, Vol.63 (6), p.881-889 [Periódico revisado por pares]

Park Ridge, IL: American Association of Neurological Surgeons

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2
Myopathy with mitochondrial abnormalities and rimmed vacuoles
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Artigo
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Myopathy with mitochondrial abnormalities and rimmed vacuoles

LEHMANN, J ; ZIEGAN, J ; OERTEL, G ; LÖSSNER, J ; KÜHN, H.-J

Acta neuropathologica, 1986, Vol.70 (1), p.86-90 [Periódico revisado por pares]

Berlin: Springer

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3
Long-term follow-up of lower lumbar fusion patients
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Artigo
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Long-term follow-up of lower lumbar fusion patients

LEHMANN, T. R ; SPRATT, K. F ; TOZZI, J. E ; WEINSTEIN, J. N ; REINARZ, S. J ; EL-KHOURY, G. Y ; COLBY, H

Spine (Philadelphia, Pa. 1976), 1987-03, Vol.12 (2), p.97-104 [Periódico revisado por pares]

Philadelphia, PA: Lippincott

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4
The excitatory amino acid antagonist kynurenic acid administered after hypoxic-ischemia in neonatal rats offers neuroprotection
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Artigo
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The excitatory amino acid antagonist kynurenic acid administered after hypoxic-ischemia in neonatal rats offers neuroprotection

Andiné, Peter ; Lehmann, Anders ; Ellrén, Katarina ; Wennberg, Elisabet ; Kjellmer, Ingemar ; Nielsen, Thorkild ; Hagberg, Henrik

Neuroscience letters, 1988-07, Vol.90 (1), p.208-212 [Periódico revisado por pares]

Shannon: Elsevier Ireland Ltd

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5
Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19
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Artigo
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Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19

Kausch, K. ; Lehmann-Horn, F. ; Janka, M. ; Wieringa, B. ; Grimm, T. ; Müller, C.R.

Genomics (San Diego, Calif.), 1991-07, Vol.10 (3), p.765-769 [Periódico revisado por pares]

San Diego, CA: Elsevier Inc

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6
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17
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Artigo
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Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17

Koch, M C ; Ricker, K ; Otto, M ; Grimm, T ; Hoffman, E P ; Rüdel, R ; Bender, K ; Zoll, B ; Harper, P S ; Lehmann-Horn, F

Journal of medical genetics, 1991-09, Vol.28 (9), p.583-586 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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7
Validation of World Health Organization guidelines for cancer pain relief during the last days and hours of life
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Artigo
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Validation of World Health Organization guidelines for cancer pain relief during the last days and hours of life

Grond, Stefan ; Zech, Detlev ; Schug, Stephan A. ; Lynch, John ; Lehmann, Klaus A.

Journal of pain and symptom management, 1991-10, Vol.6 (7), p.411-422 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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8
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17
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Artigo
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Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17

KOCH, M. C ; RICKER, K ; OTTO, M ; GRIMM, T ; BENDER, K ; ZOLL, B ; HARPER, P. S ; LEHMANN-HORN, F ; RÜDEL, R ; HOFFMAN, E. P

Human genetics, 1991-11, Vol.88 (1), p.71-74 [Periódico revisado por pares]

Heidelberg: Springer

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9
The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia
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Artigo
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The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia

Koch, Manuela C. ; Steinmeyer, Klaus ; Lorenz, Claudius ; Ricker, Kenneth ; Wolf, Friedrich ; Otto, Michael ; Zoll, Barbara ; Lehmann-Horn, Frank ; Grzeschik, Karl-Heinz ; Jentsch, Thomas J.

Science (American Association for the Advancement of Science), 1992-08, Vol.257 (5071), p.797-800 [Periódico revisado por pares]

WASHINGTON: American Society for the Advancement of Science

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10
Molecular genetic and genetic correlations in sodium channelopathies : lack of founder effect and evidence for a second gene
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Artigo
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Molecular genetic and genetic correlations in sodium channelopathies : lack of founder effect and evidence for a second gene

WANG, J ; ZHOU, J ; SILLEN, A ; MARKS, H. G ; HARTLAGE, P ; GALLOWAY, G ; RICKER, K ; LEHMANN-HORN, F ; HAYAKAWA, H ; HOFFMAN, E. P ; TODOROVIC, S. M ; FEERO, W. G ; BARANY, F ; CONWIT, R ; HAUSMANOWA-PETRUSEWICZ, I ; FIDZIANSKA, A ; ARAHATA, K ; WESSEL, H. B

American journal of human genetics, 1993-06, Vol.52 (6), p.1074-1084 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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