The role of ICP overnight monitoring (ONM) in children with suspected craniostenosis
Zipfel, J., Jager, B., Collmann, H., Czosnyka, Z., Schuhmann, M. U., Schweitzer, T.
Published in Child's nervous system (2020)
Published in Child's nervous system (2020)
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Journal Article
Avoiding CT scans in children with single-suture craniosynostosis
Schweitzer, T., Böhm, H., Meyer-Marcotty, P., Collmann, H., Ernestus, R.-I., Krauß, J.
Published in Child's nervous system (01.07.2012)
Published in Child's nervous system (01.07.2012)
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Journal Article
Neurosurgical aspects of childhood hypophosphatasia
Collmann, H, Mornet, E, Gattenlöhner, S, Beck, C, Girschick, H
Published in Child's nervous system (01.02.2009)
Published in Child's nervous system (01.02.2009)
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Journal Article
Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasia
Girschick, H J, Schneider, P, Haubitz, I, Hiort, O, Collmann, H, Beer, M, Shin, Y S, Seyberth, H W
Published in Orphanet journal of rare diseases (28.06.2006)
Published in Orphanet journal of rare diseases (28.06.2006)
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Journal Article
Neurosurgery in Würzburg until World War II
Arnold, H, Collmann, H
Published in Journal of neurological surgery. Part A, Central European neurosurgery (01.01.2012)
Published in Journal of neurological surgery. Part A, Central European neurosurgery (01.01.2012)
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Journal Article
Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome
Wieland, I, Weidner, C, Ciccone, R, Lapi, E, McDonald-McGinn, D, Kress, W, Jakubiczka, S, Collmann, H, Zuffardi, O, Zackai, E, Wieacker, P
Published in Clinical genetics (01.12.2007)
Published in Clinical genetics (01.12.2007)
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Journal Article
Morphometric analysis of untreated adult skulls in syndromic and nonsyndromic craniosynostosis
Weber, J., Collmann, H., Czarnetzki, A., Spring, A., Pusch, C. M.
Published in Neurosurgical review (01.04.2008)
Published in Neurosurgical review (01.04.2008)
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Journal Article
Hypophosphatasia
Beck, C, Morbach, H, Stenzel, M, Schneider, P, Collmann, H, Girschick, G, Girschick, H J
Published in Klinische Padiatrie (01.07.2009)
Published in Klinische Padiatrie (01.07.2009)
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Journal Article
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly
KRESS, W, PETERSEN, B, COLLMANN, H, GRIMM, T
Published in Cytogenetic and genome research (01.01.2000)
Published in Cytogenetic and genome research (01.01.2000)
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Journal Article
Management of hydrocephalus in children with plasminogen deficiency
Weinzierl, M R, Collmann, H, Korinth, M C, Gilsbach, J M, Rohde, V
Published in European journal of pediatric surgery (01.04.2007)
Published in European journal of pediatric surgery (01.04.2007)
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Journal Article
Hypophosphatasia - Recent Advances in Diagnosis and Treatment
C., Beck, H., Morbach, M., Stenzel, H., Collmann, P., Schneider, J., Girschick H.
Published in The Open bone journal (11.05.2009)
Published in The Open bone journal (11.05.2009)
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Journal Article
Recurrent bacterial meningitis
LIEB, G, KRAUSS, J, COLLMANN, H, SCHROD, L, SÖRENSEN, N
Published in European journal of pediatrics (1996)
Published in European journal of pediatrics (1996)
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Journal Article
Fetal intracranial tumors detected by ultrasound
Müller, T., Girschick, G., Mark, K., Wirbelauer, J., Klein, R., Collmann, H., Dietl, J.
Published in Ultrasound in obstetrics & gynecology (01.09.2001)
Published in Ultrasound in obstetrics & gynecology (01.09.2001)
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