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Results of search for 'au:"Kyllerman, M"', page 3 of 5
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Authors
Aronsson, M
Ben-Menachem, E
Bergström, T
Conradi, N
Darin, N
Forsgren, L
Hagberg, B
Hagberg, G
Hedström, A
Holmgren, G
Kyllerman, M
Martinsson, T
Månsson, J E
Oldfors, A
Olegård, R
Sabel, K G
Sandin, B
Sanner, G
Steffenburg, U
Wahlström, J
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Adolescent
Adult
Brain
Child
Child, Preschool
Dystonia
Epilepsies, Myoclonic
Female
Humans
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Infant, Newborn
Intellectual Disability
Male
Pedigree
Sweden
complications
diagnosis
etiology
genetics
pathology
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Swedish
Your search returned 81 results.
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41.
Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles.
[electronic resource]
by
Darin, N
Kyllerman, M
Wahlström, J
Martinsson, T
Oldfors, A
Producer:
19980825
In:
Annals of neurology
vol. 44
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42.
Early onset dystonia decreasing with development. Case report of two children with familial myoclonic dystonia.
[electronic resource]
by
Kyllerman, M
Sanner, G
Forsgren, L
Holmgren, G
Wahlström, J
Producer:
19931229
In:
Brain & development
vol. 15
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43.
Dilated cardiomyopathy and the dystrophin gene: an illustrated review.
[electronic resource]
by
Oldfors, A
Eriksson, B O
Kyllerman, M
Martinsson, T
Wahlström, J
Producer:
19950301
In:
British heart journal
vol. 72
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44.
Late cerebral graft versus host reaction in a bone marrow transplanted girl with Hurler (MPS I) disease.
[electronic resource]
by
Kyllerman, M
Himmelmann, K
Fasth, A
Nordborg, C
Månsson, J-E
Producer:
20090511
In:
Neuropediatrics
vol. 39
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45.
An outbreak of Coxsackie virus type B2 among neonates in an obstetrical ward.
[electronic resource]
by
Eilard, T
Kyllerman, M
Wennerblom, I
Eeg-Olofsson, O
Lycke, E
Producer:
19740722
In:
Acta paediatrica Scandinavica
vol. 63
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46.
Children of alcoholic mothers. Developmental, perceptual and behavioural characteristics as compared to matched controls.
[electronic resource]
by
Aronson, M
Kyllerman, M
Sabel, K G
Sandin, B
Olegård, R
Producer:
19850513
In:
Acta paediatrica Scandinavica
vol. 74
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47.
Infantile galactosialidosis presenting with congenital adrenal hyperplasia and renal hypertension.
[electronic resource]
by
Kyllerman, M
Månsson, J E
Westphal, O
Conradi, N
Nellström, H
Producer:
19931203
In:
Pediatric neurology
vol. 9
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48.
Aicardi syndrome: follow-up investigation of Swedish children born in 1975-2002.
[electronic resource]
by
Palmér, L
Zetterlund, B
Hård, A-L
Steneryd, K
Kyllerman, M
Producer:
20080314
In:
Neuropediatrics
vol. 38
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49.
PCR diagnosis of primary herpesvirus type I in poliomyelitis-like paralysis and respiratory tract disease.
[electronic resource]
by
Kyllerman, M G
Herner, S
Bergström, T B
Ekholm, S E
Producer:
19930922
In:
Pediatric neurology
vol. 9
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50.
X-linked myotubular myopathy: clinical and pathological findings in a family.
[electronic resource]
by
Oldfors, A
Kyllerman, M
Wahlström, J
Darnfors, C
Henriksson, K G
Producer:
19891004
In:
Clinical genetics
vol. 36
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51.
Aicardi syndrome: presentation at onset in Swedish children born in 1975-2002.
[electronic resource]
by
Palmér, L
Zetterlund, B
Hård, A-L
Steneryd, K
Kyllerman, M
Producer:
20061031
In:
Neuropediatrics
vol. 37
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52.
Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1.
[electronic resource]
by
Martinsson, T
Darin, N
Kyllerman, M
Oldfors, A
Hallberg, B
Wahlström, J
Producer:
19990520
In:
American journal of human genetics
vol. 64
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53.
Dyskinetic cerebral palsy. I. Clinical categories, associated neurological abnormalities and incidences.
[electronic resource]
by
Kyllerman, M
Bager, B
Bensch, J
Bille, B
Olow, I
Voss, H
Producer:
19821218
In:
Acta paediatrica Scandinavica
vol. 71
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54.
Rapidly progressive type III Gaucher disease: deterioration following partial splenectomy.
[electronic resource]
by
Kyllerman, M
Conradi, N
Månsson, J E
Percy, A K
Svennerholm, L
Producer:
19900711
In:
Acta paediatrica Scandinavica
vol. 79
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55.
Central nervous system malformations and white matter changes in pseudo-neonatal adrenoleukodystrophy.
[electronic resource]
by
Kyllerman, M
Blomstrand, S
Månsson, J E
Conradi, N G
Hindmarsh, T
Producer:
19910404
In:
Neuropediatrics
vol. 21
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56.
Diagnosis of Epstein-Barr virus-induced central nervous system infections by DNA amplification from cerebrospinal fluid.
[electronic resource]
by
Landgren, M
Kyllerman, M
Bergström, T
Dotevall, L
Ljungström, L
Ricksten, A
Producer:
19940609
In:
Annals of neurology
vol. 35
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57.
Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy.
[electronic resource]
by
Jansson, M
Darin, N
Kyllerman, M
Martinsson, T
Wahlström, J
Oldfors, A
Producer:
20001207
In:
Acta neuropathologica
vol. 100
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58.
Late-infantile Gaucher disease in a child with myoclonus and bulbar signs: neuropathological and neurochemical findings.
[electronic resource]
by
Conradi, N
Kyllerman, M
Månsson, J E
Percy, A K
Svennerholm, L
Producer:
19911113
In:
Acta neuropathologica
vol. 82
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59.
Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation.
[electronic resource]
by
Kyllerman, M
Forsgren, L
Sanner, G
Holmgren, G
Wahlström, J
Drugge, U
Producer:
19910128
In:
Movement disorders : official journal of the Movement Disorder Society
vol. 5
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60.
[Adrenoleukodystrophy. A disease of current interest and many aspects].
[electronic resource]
by
Kyllerman, M
Blennow, G
Månsson, J E
Wahlström, J
von Döbeln, U
Producer:
19940222
In:
Lakartidningen
vol. 91
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