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Results of search for 'au:"Boltshauser, E"', page 9 of 11
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Authors
Boesch, C
Boltshauser, E
Briner, J
Bucher, H U
Deonna, T
Eich, G
Fanconi, S
Huisman, T A G M
Isler, W
Martin, E
Molinari, L
Nadal, D
Poretti, A
Schinzel, A
Schmitt, B
Steinlin, M
Superti-Furga, A
Thun-Hohenstein, L
Valavanis, A
Wohlrab, G
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Adolescent
Adult
Brain
Cerebellum
Child
Child, Preschool
Female
Follow-Up Studies
Humans
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Infant, Newborn
Magnetic Resonance Imaging
Male
Syndrome
abnormalities
complications
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etiology
genetics
pathology
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161.
[Long-term course in congenital analgesia].
[electronic resource]
by
Losa, M
Scheier, H
Rohner, P
Sailer, H
Hayek, J
Giedion, A
Boltshauser, E
Producer:
19900111
In:
Schweizerische medizinische Wochenschrift
vol. 119
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162.
Lhermitte-Duclos disease in 3 children: a clinical long-term observation.
[electronic resource]
by
Capone Mori, A
Hoeltzenbein, M
Poetsch, M
Schneider, J F
Brandner, S
Boltshauser, E
Producer:
20030813
In:
Neuropediatrics
vol. 34
Online resources:
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163.
Normal cognitive functions in joubert syndrome.
[electronic resource]
by
Poretti, A
Dietrich Alber, F
Brancati, F
Dallapiccola, B
Valente, E M
Boltshauser, E
Producer:
20100812
In:
Neuropediatrics
vol. 40
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164.
[Molecular genetics diagnosis of Steinert's myotonic dystrophy].
[electronic resource]
by
Spiegel, R
Einschenk, I
Schinzel, A
Shelbourne, P
Johnson, K
Boltshauser, E
Schmid, W
Producer:
19921119
In:
Schweizerische medizinische Wochenschrift
vol. 122
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165.
Interpeduncular heterotopia in Joubert syndrome: a previously undescribed MR finding.
[electronic resource]
by
Harting, I
Kotzaeridou, U
Poretti, A
Seitz, A
Pietz, J
Bendszus, M
Boltshauser, E
Producer:
20111213
In:
AJNR. American journal of neuroradiology
vol. 32
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166.
Follow-up of a child with hypoacetylaspartia.
[electronic resource]
by
Boltshauser, E
Schmitt, B
Wevers, R A
Engelke, U
Burlina, A B
Burlina, A P
Producer:
20041130
In:
Neuropediatrics
vol. 35
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167.
Moyamoya disease and Moyamoya syndrome: experience in Europe; choice of revascularisation procedures.
[electronic resource]
by
Khan, N
Schuknecht, B
Boltshauser, E
Capone, A
Buck, A
Imhof, H G
Yonekawa, Y
Producer:
20040831
In:
Acta neurochirurgica
vol. 145
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168.
Homozygosity mapping of a third Joubert syndrome locus to 6q23.
[electronic resource]
by
Lagier-Tourenne, C
Boltshauser, E
Breivik, N
Gribaa, M
Bétard, C
Barbot, C
Koenig, M
Producer:
20040507
In:
Journal of medical genetics
vol. 41
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169.
MRI following severe perinatal asphyxia: preliminary experience.
[electronic resource]
by
Steinlin, M
Dirr, R
Martin, E
Boesch, C
Largo, R H
Fanconi, S
Boltshauser, E
Producer:
19911001
In:
Pediatric neurology
vol. 7
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170.
Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: a case for "lumping".
[electronic resource]
by
Superti-Furga, A
Tenconi, R
Clementi, M
Eich, G
Steinmann, B
Boltshauser, E
Giedion, A
Producer:
19980924
In:
American journal of medical genetics
vol. 78
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171.
Outcome of medulloblastoma in children: long-term complications and quality of life.
[electronic resource]
by
Ribi, K
Relly, C
Landolt, M A
Alber, F D
Boltshauser, E
Grotzer, M A
Producer:
20060412
In:
Neuropediatrics
vol. 36
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172.
Outcome in children with brain tumours diagnosed in the first year of life: long-term complications and quality of life.
[electronic resource]
by
Gerber, N U
Zehnder, D
Zuzak, T J
Poretti, A
Boltshauser, E
Grotzer, M A
Producer:
20080721
In:
Archives of disease in childhood
vol. 93
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173.
[Magnetic resonance in pediatric research and clinical practice. II. Studies on the development and pathology of the brain in neonates, infants and young children].
[electronic resource]
by
Martin, E
Boesch, C
Grütter, R
Kikinis, R
Kewitz, G
Boltshauser, E
Werner, B
Eich, G
Producer:
19881123
In:
Helvetica paediatrica acta
vol. 43
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174.
Preclinical and manifest diabetes mellitus in young patients with Friedreich's ataxia: no evidence of immune process behind the islet cell destruction.
[electronic resource]
by
Schoenle, E J
Boltshauser, E J
Baekkeskov, S
Landin Olsson, M
Torresani, T
von Felten, A
Producer:
19890908
In:
Diabetologia
vol. 32
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175.
Follow-up of optic pathway gliomas in children with neurofibromatosis type 1.
[electronic resource]
by
Kuenzle, C
Weissert, M
Roulet, E
Bode, H
Schefer, S
Huisman, T
Landau, K
Boltshauser, E
Producer:
19950706
In:
Neuropediatrics
vol. 25
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176.
A syndrome of primary combined immunodeficiency with microcephaly, cerebellar hypoplasia, growth failure and progressive pancytopenia.
[electronic resource]
by
Berthet, F
Caduff, R
Schaad, U B
Roten, H
Tuchschmid, P
Boltshauser, E
Seger, R A
Producer:
19940816
In:
European journal of pediatrics
vol. 153
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177.
Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR.
[electronic resource]
by
Kleinle, S
Wiesmann, U
Superti-Furga, A
Krähenbühl, S
Boltshauser, E
Reichen, J
Liechti-Gallati, S
Producer:
19971119
In:
Human genetics
vol. 100
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178.
Ophthalmological findings in Joubert syndrome.
[electronic resource]
by
Sturm, V
Leiba, H
Menke, M N
Valente, E M
Poretti, A
Landau, K
Boltshauser, E
Producer:
20110418
In:
Eye (London, England)
vol. 24
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179.
MR imaging of brain maturation in normal and developmentally handicapped children.
[electronic resource]
by
Martin, E
Boesch, C
Zuerrer, M
Kikinis, R
Molinari, L
Kaelin, P
Boltshauser, E
Duc, G
Producer:
19901017
In:
Journal of computer assisted tomography
vol. 14
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180.
X-linked centronuclear myopathy: mapping the gene to Xq28.
[electronic resource]
by
Liechti-Gallati, S
Müller, B
Grimm, T
Kress, W
Müller, C
Boltshauser, E
Moser, H
Braga, S
Producer:
19920904
In:
Neuromuscular disorders : NMD
vol. 1
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