The role of ICP overnight monitoring (ONM) in children with suspected craniostenosis von Zipfel, J., Jager, B., Collmann, H., Czosnyka, Z., Schuhmann, M. U., Schweitzer, T.

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Hydrocephalus in craniosynostosis: a review von Collmann, H, Sörensen, N, Krauss, J

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Avoiding CT scans in children with single-suture craniosynostosis von Schweitzer, T., Böhm, H., Meyer-Marcotty, P., Collmann, H., Ernestus, R.-I., Krauß, J.

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Neurosurgical aspects of childhood hypophosphatasia von Collmann, H, Mornet, E, Gattenlöhner, S, Beck, C, Girschick, H

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Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasia von Girschick, H J, Schneider, P, Haubitz, I, Hiort, O, Collmann, H, Beer, M, Shin, Y S, Seyberth, H W

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Cutaneous lesions in occult spinal dysraphism--correlation with intraspinal findings von Schropp, C, Sörensen, N, Collmann, H, Krauss, J

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Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome von Wieland, I, Weidner, C, Ciccone, R, Lapi, E, McDonald-McGinn, D, Kress, W, Jakubiczka, S, Collmann, H, Zuffardi, O, Zackai, E, Wieacker, P

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Morphometric analysis of untreated adult skulls in syndromic and nonsyndromic craniosynostosis von Weber, J., Collmann, H., Czarnetzki, A., Spring, A., Pusch, C. M.

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Radiographic changes in non-operated isolated sagittal suture synostosis von Fisher, M, Collmann, H, Darge, K

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An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly von Kress, W., Petersen, B., Collmann, H., Grimm, T.

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Management of Hydrocephalus in Children with Plasminogen Deficiency von Weinzierl, M. R., Collmann, H., Korinth, M. C., Gilsbach, J. M., Rohde, V.

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Saethre-Chotzen Syndrome: Clinical and Molecular Genetic Aspects von Kress, W., Collmann, H.

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Nonsyndromic Craniosynostoses von Collmann, H., Solomon, B.D., Schweitzer, T., Kress, W., Muenke, M.

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Apert, Crouzon, and Pfeiffer Syndromes von Michael Cohen Jr, M.M.

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Craniosynostosis and Chromosomal Alterations von Passos-Bueno, M.R., Fanganiello, R.D., Jehee, F.S.

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Molecular Genetic Testing of Patients with Craniosynostosis von Hehr, U.

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Signal Transduction Pathways and Their Impairment in Syndromic Craniosynostosis von Connerney, J.J., Spicer, D.B.

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Imaging Studies and Neurosurgical Treatment von Collmann, H., Schweitzer, T., Böhm, H.

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Muenke Syndrome von Solomon, B.D., Muenke, M.

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Craniofrontonasal Syndrome: Molecular Genetics, EFNB1 Mutations and the Concept of Cellular Interference von Wieland, I.

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