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I Mutz

Showing results (51-60 of 82) with videos related to

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Clinical Dysmorphology|January 29, 2000
Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISHE Petek, G Köstl, I Mutz, et al.
Archives of Disease in Childhood|April 24, 2001
A prospective evaluation of community acquired gastroenteritis in paediatric practices: impact and disease burden of rotavirus infectionM Frühwirth, W Karmaus, I Moll-Schüler, et al.
Padiatrie Und Padologie|January 1, 1986
[Results of neuroblastoma treatment in Austria (1979-1984)]I Mutz, C Urban, H Gadner, et al.
Clinical Genetics|May 1, 1986
Infantile type of sialic acid storage disease with sialuriaE Paschke, G Trinkl, W Erwa, et al.
Wiener Klinische Wochenschrift|January 1, 1991
[Endocrinologic function following cranial irradiation in acute lymphoblastic leukemia in childhood]H Lackner, J Schwingshandl, B Pakisch, et al.
Pediatric Research|September 1, 1985
The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detectionA Roscher, B Molzer, H Bernheimer, et al.
European Journal of Pediatrics|February 1, 1994
Neonatal allo-immune thrombocytopenia due to fetomaternal HPA-1 incompatibility of a homozygous HPA-1a mother and a homozygous HPA-1b father. A case reportR Moser, I Fae, A Neumeister, et al.
The Journal of the Oklahoma State Medical Association|January 1, 1979
Pediatric grand rounds: OsteomyelitisA MacADAM, H D Riley, J Vanhoutte, et al.
Journal of Clinical Microbiology|May 2, 2000
Distribution of rotavirus VP4 genotypes and VP7 serotypes among nonhospitalized and hospitalized patients with gastroenteritis and patients with nosocomially acquired gastroenteritis in AustriaM Frühwirth, S Brösl, H Ellemunter, et al.
Clinical Dysmorphology|April 20, 2001
Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter)E Petek, G Köstl, L Rauter, et al.
Pageof 9

Showing results (51-60 of 82) with videos related to

Sort By:
Pageof 9
Clinical Dysmorphology|January 29, 2000
Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISHE Petek, G Köstl, I Mutz, et al.
Archives of Disease in Childhood|April 24, 2001
A prospective evaluation of community acquired gastroenteritis in paediatric practices: impact and disease burden of rotavirus infectionM Frühwirth, W Karmaus, I Moll-Schüler, et al.
Padiatrie Und Padologie|January 1, 1986
[Results of neuroblastoma treatment in Austria (1979-1984)]I Mutz, C Urban, H Gadner, et al.
Clinical Genetics|May 1, 1986
Infantile type of sialic acid storage disease with sialuriaE Paschke, G Trinkl, W Erwa, et al.
Wiener Klinische Wochenschrift|January 1, 1991
[Endocrinologic function following cranial irradiation in acute lymphoblastic leukemia in childhood]H Lackner, J Schwingshandl, B Pakisch, et al.
Pediatric Research|September 1, 1985
The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detectionA Roscher, B Molzer, H Bernheimer, et al.
European Journal of Pediatrics|February 1, 1994
Neonatal allo-immune thrombocytopenia due to fetomaternal HPA-1 incompatibility of a homozygous HPA-1a mother and a homozygous HPA-1b father. A case reportR Moser, I Fae, A Neumeister, et al.
The Journal of the Oklahoma State Medical Association|January 1, 1979
Pediatric grand rounds: OsteomyelitisA MacADAM, H D Riley, J Vanhoutte, et al.
Journal of Clinical Microbiology|May 2, 2000
Distribution of rotavirus VP4 genotypes and VP7 serotypes among nonhospitalized and hospitalized patients with gastroenteritis and patients with nosocomially acquired gastroenteritis in AustriaM Frühwirth, S Brösl, H Ellemunter, et al.
Clinical Dysmorphology|April 20, 2001
Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter)E Petek, G Köstl, L Rauter, et al.
Pageof 9