Suchergebnisse - "Kumlien, Eva"

PubPharm (110)

81

SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration

enthalten in: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2009

von Orlén, H. | Melberg, A. | Raininko, R. | +10

82

Incomplete hippocampal inversion—is there a relation to epilepsy?

enthalten in: European radiology | 2009

von Bajic, D. | Kumlien, E. | Mattsson, P. | +3

83

Incomplete hippocampal inversion—is there a relation to epilepsy?

enthalten in: European radiology | 2009

von Bajic, D. | Kumlien, E. | Mattsson, P. | +3

84

Incomplete hippocampal inversion—is there a relation to epilepsy?

enthalten in: European radiology | 2009

von Bajic, D. | Kumlien, E. | Mattsson, P. | +3

85

DLG3/SAP102 protein expression in malformations of cortical development : a study of human epileptic cortex by tissue microarray

enthalten in: Epilepsy research | 2009

von Qu, M. | Aronica, E. | Boer, K. | +6

86

DLG3/SAP102 protein expression in malformations of cortical development: A study of human epileptic cortex by tissue microarray

enthalten in: Epilepsy research | 2009

von Qu, M. | Aronica, E. | Boer, K. | +6

87

DLG3-SAP102 protein expression in malformations of cortical development: A study of human epileptic cortex by tissue microarray

enthalten in: Epilepsy research | 2009

von Qu, M. | Aronica, E. | Boer, K. | +6

88

SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degenerationHanna Örlén and Atle Melberg contributed equally to this study.How to Cite this Article: Örlén H, Melberg A, Raininko R, Kumlien E, Entesarian M, Söderberg P, Påhlman M, Darin N, Kyllerman M, Holmberg E, Engler H, Eriksson U, Dahl N. 2009. SPG11 Mutations Cause Kjellin Syndrome, a Hereditary Spastic Paraplegia With Thin Corpus Callosum and Central Retinal Degeneration. Am J Med Genet Part B 150B:984-992.

enthalten in: American journal of medical genetics / B | 2009

von Örlén, H. | Melberg, A. | Raininko, R. | +10

89

Incomplete hippocampal inversion—is there a relation to epilepsy?

enthalten in: European radiology | 2009

von Bajic, D. | Kumlien, E. | Mattsson, P. | +3

90

Response - Editorial. Subarachnoid hemorrhage and microdialysis.

enthalten in: Journal of neurosurgery | 2009

von Samuelsson, C. | Howells, T. | Kumlien, E. | +3