Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: FATHER, . Treffer: 42
2023
Michael, S; Borgmann-Staudt, A; Sommerhäuser, G; Kepakova, K; Klco-Brosius, S; Kruseova, J; Nagele, E; Panasiuk, A; Vetsch, J; Balcerek, M
Educational pathways of childhood cancer survivors-a parental cohort.
J Cancer Surviv. 2023; 17(2):518-525
Doi: 10.1007/s11764-022-01303-y
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2022
Versele, V; Dieberger, A; van, Poppel, M; Van, De, Maele, K; Deliens, T; Aerenhouts, D; Clarys, P; Devlieger, R; Bogaerts, A
The influence of parental body composition and lifestyle on offspring growth trajectories.
Pediatr Obes. 2022; e12929
Doi: 10.1111/ijpo.12929
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2020
Mozun, R; Ardura-Garcia, C; de, Jong, CCM; Goutaki, M; Usemann, J; Singer, F; Latzin, P; Kuehni, CE; Moeller, A
Cigarette, shisha, and electronic smoking and respiratory symptoms in Swiss children: The LUIS study.
Pediatr Pulmonol. 2020; 55(10):2806-2815
Doi: 10.1002/ppul.24985
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Resch, B; Hofbauer-Krug, C; Pansy, J; Prechtl, K; Avian, A; Kurz, R
Prospective Randomized Observational Pilot Trial Evaluating the Effect of Different Durations of Interdisciplinary Early Intervention and Family Support in Parents of Very Low Birth Weight Infants (Early Bird Study).
Front Public Health. 2020; 8:242
Doi: 10.3389/fpubh.2020.00242
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2019
Coi, A; Santoro, M; Garne, E; Pierini, A; Addor, MC; Alessandri, JL; Bergman, JEH; Bianchi, F; Boban, L; Braz, P; Cavero-Carbonell, C; Gatt, M; Haeusler, M; Klungsøyr, K; Kurinczuk, JJ; Lanzoni, M; Lelong, N; Luyt, K; Mokoroa, O; Mullaney, C; Nelen, V; Neville, AJ; O'Mahony, MT; Perthus, I; Rankin, J; Rissmann, A; Rouget, F; Schaub, B; Tucker, D; Wellesley, D; Wisniewska, K; Zymak-Zakutnia, N; Barišić, I
Epidemiology of achondroplasia: A population-based study in Europe.
AM J MED GENET A. 2019; 179(9): 1791-1798.
Doi: 10.1002/ajmg.a.61289
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Pichler-Stachl, E; Urlesberger, P; Mattersberger, C; Baik-Schneditz, N; Schwaberger, B; Urlesberger, B; Pichler, G
Parental Stress Experience and Age of Mothers and Fathers After Preterm Birth and Admission of Their Neonate to Neonatal Intensive Care Unit; A Prospective Observational Pilot Study.
Front Pediatr. 2019; 7: 439-439.
Doi: 10.3389/fped.2019.00439
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2016
Alexandrowicz, RW; König, D; Unger, A; Klug, G; Soulier, N; Freidl, M; Friedrich, F
[Depression Symptoms of Mothers and Fathers of Persons with Schizophrenia].
Psychiatr Prax. 2016; 43(4): 213-218.
Doi: 10.1055/s-0035-1552629
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Schwarz, C; Lawitschka, A; Böhmig, GA; Dauber, EM; Greinix, H; Kozakowski, N; Mühlbacher, F; Berlakovich, GA; Wekerle, T
Kidney Transplantation With Corticosteroids Alone After Haploidentical HSCT From The Same Donor.
Transplantation. 2016; 100(10):2219-2221
Doi: 10.1097/TP.0000000000001213
(- Case Report)
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2015
Friedrich, F; Gross, R; Wrobel, M; Klug, G; Unger, A; Fellinger, M; Süßenbacher, S; Freidl, M; Saumer, G; Wancata, J
[Burden of mothers and fathers of persons with schizophrenia].
Psychiatr Prax. 2015; 42(4):208-215
Doi: 10.1055/s-0034-1370080
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von Wurmb-Schwark, N; Podruks, E; Schwark, T; Göpel, W; Fimmers, R; Poetsch, M
About the power of biostatistics in sibling analysis-comparison of empirical and simulated data.
Int J Legal Med. 2015; 129(6):1201-1209
Doi: 10.1007/s00414-015-1252-9
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2014
Al Kaissi, A; Ganger, R; Rötzer, KM; Klaushofer, K; Grill, F
A child with split-hand/foot associated with tibial hemimelia (SHFLD syndrome) and thrombocytopenia maps to chromosome region 17p13.3.
Am J Med Genet A. 2014; 164A(9):2338-2343
Doi: 10.1002/ajmg.a.36614
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Mautner, E; Ashida, C; Greimel, E; Lang, U; Kolman, C; Alton, D; Inoue, W
Are there differences in the health outcomes of mothers in Europe and East-Asia? A cross-cultural health survey.
Biomed Res Int. 2014; 2014:856543-856543
Doi: 10.1155/2014/856543
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2013
Beck, BB; Baasner, A; Buescher, A; Habbig, S; Reintjes, N; Kemper, MJ; Sikora, P; Mache, C; Pohl, M; Stahl, M; Toenshoff, B; Pape, L; Fehrenbach, H; Jacob, DE; Grohe, B; Wolf, MT; Nürnberg, G; Yigit, G; Salido, EC; Hoppe, B
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies.
Eur J Hum Genet. 2013; 21(2):162-172
Doi: 10.1038/ejhg.2012.139
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Poetsch, M; Preusse-Prange, A; Schwark, T; von Wurmb-Schwark, N
The new guidelines for paternity analysis in Germany-how many STR loci are necessary when investigating duo cases?
Int J Legal Med. 2013; 127(4): 731-734.
Doi: 10.1007/s00414-013-0867-y
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2011
Al Kaissi, A; M Roetzer, K; Ulz, P; Heitzer, E; Klaushofer, K; Grill, F
Extra phenotypic features in a girl with Miller syndrome.
Clin Dysmorphol. 2011; 20(2): 66-72.
Doi: 10.1097/MCD.0b013e3283416701
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2010
Sovinz, P; Urban, C; Uhrig, S; Stepan, V; Lackner, H; Schwinger, W; Benesch, M; Moser, A; Spuller, E; Speicher, MR
Pheochromocytoma in a 2.75-year-old-girl with a germline von Hippel-Lindau mutation Q164R.
Am J Med Genet A. 2010; 152A(7): 1752-1755.
Doi: 10.1002/ajmg.a.33407
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2009
Music, I; Novak, M; Acham-Roschitz, B; Muntean, W
Screening for haemorrhagic disorders in paediatric patients by means of a questionnaire.
Hamostaseologie. 2009; 29 Suppl 1: S87-S89.
Doi: 10.1055/s-0037-1621503
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2008
Jenewein, J; Moergeli, H; Fauchère, JC; Bucher, HU; Kraemer, B; Wittmann, L; Schnyder, U; Büchi, S
Parents' mental health after the birth of an extremely preterm child: a comparison between bereaved and non-bereaved parents.
J Psychosom Obstet Gynaecol. 2008; 29(1):53-60
Doi: 10.1080/01674820701640181
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Margreiter, C; Aigner, F; Orozco, H; Wechselberger, G; Ollinger, R; Bösmüller, C; Sucher, R; Mark, W; Margreiter, R
Hepatic artery reconstruction with inferior mesenteric vein graft in pediatric living donor liver transplantation.
Pediatr Transplant. 2008; 12(3):324-8
Doi: 10.1111/j.1399-3046.2007.00868.x
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Schulz, AL; Albrecht, B; Arici, C; van der Burgt, I; Buske, A; Gillessen-Kaesbach, G; Heller, R; Horn, D; Hübner, CA; Korenke, GC; König, R; Kress, W; Krüger, G; Meinecke, P; Mücke, J; Plecko, B; Rossier, E; Schinzel, A; Schulze, A; Seemanova, E; Seidel, H; Spranger, S; Tuysuz, B; Uhrig, S; Wieczorek, D; Kutsche, K; Zenker, M
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.
Clin Genet. 2008; 73(1):62-70
Doi: 10.1111/j.1399-0004.2007.00931.x
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2007
Büchi, S; Mörgeli, H; Schnyder, U; Jenewein, J; Hepp, U; Jina, E; Neuhaus, R; Fauchère, JC; Bucher, HU; Sensky, T
Grief and post-traumatic growth in parents 2-6 years after the death of their extremely premature baby.
Psychother Psychosom. 2007; 76(2):106-114
Doi: 10.1159/000097969
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Guddat, SS; Schalinski, S; Püschel, K; Tsokos, M; Schulz, F
[An extreme case of undoing and posing in a case of murder-suicide. A forensic pathological approach to crime scene investigation].
Arch Kriminol. 2007; 220(1-2): 20-4.
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Mach, M; Windpassinger, C; Wagner, K; Kroisel, PM; Petek, E
Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
GENET COUNSEL. 2007; 18(1): 9-16.
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2006
Fauth, C; Gribble, SM; Porter, KM; Codina-Pascual, M; Ng, BL; Kraus, J; Uhrig, S; Leifheit, J; Haaf, T; Fiegler, H; Carter, NP; Speicher, MR
Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.
Hum Genet. 2006; 119(1-2):145-153
Doi: 10.1007/s00439-005-0103-z
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Hörl, G; Kroisel, PM; Wagner, E; Tiran, B; Petek, E; Steyrer, E
Compound heterozygosity (G71R/R140H) in the lecithin:cholesterol acyltransferase (LCAT) gene results in an intermediate phenotype between LCAT-deficiency and fish-eye disease.
Atherosclerosis. 2006; 187(1): 101-109.
Doi: 10.1016/j.atherosclerosis.2005.08.038
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Schwarzbraun, T; Ullmann, R; Schubert, M; Ledinegg, M; Ofner, L; Windpassinger, C; Wagner, K; Kroisel, PM; Petek, E
Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development.
Cytogenet Genome Res. 2006; 115(1):84-89
Doi: 10.1159/000094804
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Stompe, T; Strnad, A; Ritter, K; Fischer-Danzinger, D; Letmaier, M; Ortwein-Swoboda, G; Schanda, H
Family and social influences on offending in men with schizophrenia.
Aust N Z J Psychiatry. 2006; 40(6-7):554-560
Doi: 10.1111/j.1440-1614.2006.01838.x
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2005
Drexler, C; Glock, B; Vadon, M; Staudacher, E; Dauber, EM; Ulrich, S; Reisacher, RB; Mayr, WR; Lanzer, G; Wagner, T
Tetragametic chimerism detected in a healthy woman with mixed-field agglutination reactions in ABO blood grouping.
TRANSFUSION. 2005; 45(5): 698-703.
Doi: 10.1111/j.1537-2995.2005.04304.x
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Reich, O; Regauer, S
Endometrial stromal sarcoma--observational evidence of a genetic background?
Eur J Gynaecol Oncol. 2005; 26(3):288-290
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2004
Mehrabi, A; Kashfi, A; Tonshoff, B; Feneberg, R; Mehls, O; Schemmer, P; Kraus, T; Wiesel, M; Buchler, MW; Schmidt, J
Long-term results of paediatric kidney transplantation at the University of Heidelberg: a 35 year single-centre experience
NEPHROL DIAL TRANSPL. 2004; 19: 69-74.
Doi: 10.1093/ndt/gfh1046
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Nickel, MK; Tritt, K; Mitterlehner, FO; Leiberich, P; Nickel, C; Lahmann, C; Forthuber, P; Rother, WK; Loew, TH
Sexual abuse in childhood and youth as psychopathologically relevant life occurrence: cross-sectional survey.
Croat Med J. 2004; 45(4):483-489
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2003
Kahofer, P; Bruckner-Tuderman, L; Metze, D; Lemmink, H; Scheffer, H; Smolle, J
Dystrophic epidermolysis bullosa inversa with COL7A1 mutations and absence of GDA-J/F3 protein.
Pediatr Dermatol. 2003; 20(3):243-248
Doi: 10.1046/j.1525-1470.2003.20312.x
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2002
Mache, CJ; Preisegger, KH; Kopp, S; Ratschek, M; Ring, E
De novo HNF-1 beta gene mutation in familial hypoplastic glomerulocystic kidney disease.
Pediatr Nephrol. 2002; 17(12):1021-1026
Doi: 10.1007/s00467-002-0975-2
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2001
Nelson, EA; Taylor, BJ and the ICCPS Study Group with Einspieler, C
International Child Care Practices Study: infant sleep position and parental smoking.
EARLY HUM DEV. 2001; 64(1): 7-20.
Doi: 10.1016%2FS0378-3782%2801%2900165-7
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2000
Buiting, K; Färber, C; Kroisel, P; Wagner, K; Brueton, L; Robertson, ME; Lich, C; Horsthemke, B
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counseling.
Clin Genet. 2000; 58(4):284-290
Doi: 10.1034/j.1399-0004.2000.580406.x
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Nauck, MS; Scharnagl, H; Nissen, H; Schürmann, C; Matern, D; Nauck, MA; Wieland, H; März, W; Mattern, D
FH-Freiburg: a novel missense mutation (C317Y) in growth factor repeat A of the low density lipoprotein receptor gene in a German patient with homozygous familial hypercholesterolemia.
ATHEROSCLEROSIS 2000 151: 525-534.
Doi: 10.1016/S0021-9150(99)00415-3
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1999
Halbmayer, WM; Kalhs, T; Haushofer, A; Breier, F; Fischer, M
Venous thromboembolism at a young age in a brother and sister with coinheritance of homozygous 20210A/A prothrombin mutation and heterozygous 1691G/A factor V Leiden mutation.
Blood Coagul Fibrinolysis. 1999; 10(5):297-302
Doi: 10.1097/00001721-199907000-00012
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1998
Brinckmann, J; Açil, Y; Feshchenko, S; Katzer, E; Brenner, R; Kulozik, A; Kügler, S
Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C).
Arch Dermatol Res. 1998; 290(4):181-186
Doi: 10.1007/s004030050287
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Leithner, A; Windhager, R; Kainberger, F; Lang, S
A case of aneurysmal bone cyst in father and son.
Eur J Radiol. 1998; 29(1):28-30
Doi: 10.1016/S0720-048X(98)00016-3
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1997
Diaz, MN; O'Neill, TW; Silman, AJ; and European Vertebral Osteoporosis Study Group
The influence of family history of hip fracture on the risk of vertebral deformity in men and women: the European Vertebral Osteoporosis Study.
Bone. 1997; 20(2): 145-149.
Doi: 10.1016/S8756-3282(96)00331-6
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1993
Mayer, C; Kapfhammer, HP
Couvade syndrome, a psychogenic illness in the transition to fatherhood
Fortschr Neurol Psychiatr. 1993; 61(10): 354-360.
Doi: 10.1055/s-2007-999105
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1988
Hoefler, G; Harnoncourt, F; Paschke, E; Mirtl, W; Pfeiffer, KH; Kostner, GM
Lipoprotein Lp(a). A risk factor for myocardial infarction.
ARTERIOSCLEROSIS-J VASC BIOL. 1988; 8(4): 398-401.
Doi: 10.1161/01.ATV.8.4.398
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