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Results: 1-25 | 26-50 | 51-51
Results: 26-50/51
Identity development in adulthood: A longitudinal study
Authors: Pulkkinen, L Kokko, K
Citation: L. Pulkkinen et K. Kokko, Identity development in adulthood: A longitudinal study, J RES PERS, 34(4), 2000, pp. 445-470
Herlitz junctional epidermolysis bullosa: Novel and recurrent mutations inthe LAMB3 gene and the population carrier frequency
Authors: Nakano, A Pfendner, E Pulkkinen, L Hashimoto, I Uitto, J
Citation: A. Nakano et al., Herlitz junctional epidermolysis bullosa: Novel and recurrent mutations inthe LAMB3 gene and the population carrier frequency, J INVES DER, 115(3), 2000, pp. 493-498
Complete paternal uniparental isodisomy of chromosome 1: A novel mechanismfor Herlitz junctional epidermolysis bullosa
Authors: Takizawa, Y Pulkkinen, L Chao, SC Nakajima, H Nakano, Y Shimizu, H Uitto, J
Citation: Y. Takizawa et al., Complete paternal uniparental isodisomy of chromosome 1: A novel mechanismfor Herlitz junctional epidermolysis bullosa, J INVES DER, 115(2), 2000, pp. 307-311
Epidermolysis bullosa simplex associated with severe mucous membrane involvement and novel mutations in the plectin gene
Authors: Kunz, ME Rouan, F Pulkkinen, L Hamm, H Jeschke, R Bruckner-Tuderman, L Brocker, EB Wiche, G Uitto, J Zillikens, D
Citation: Me. Kunz et al., Epidermolysis bullosa simplex associated with severe mucous membrane involvement and novel mutations in the plectin gene, J INVES DER, 114(2), 2000, pp. 376-380
Epidermolysis bullosa: Novel and de novo premature termination codon and deletion mutations in the plectin gene predict late-onset muscular dystrophy
Authors: Rouan, F Pulkkinen, L Meneguzzi, G LaForgia, S Hyde, P Kim, DU Richard, G Uitto, J
Citation: F. Rouan et al., Epidermolysis bullosa: Novel and de novo premature termination codon and deletion mutations in the plectin gene predict late-onset muscular dystrophy, J INVES DER, 114(2), 2000, pp. 381-387
Aggression in childhood and long-term unemployment in adulthood: A cycle of maladaptation and some protective factors
Authors: Kokko, K Pulkkinen, L
Citation: K. Kokko et L. Pulkkinen, Aggression in childhood and long-term unemployment in adulthood: A cycle of maladaptation and some protective factors, DEVEL PSYCH, 36(4), 2000, pp. 463-472
Epidermolysis bullosa in Mexico
Authors: Uitto, J Pulkkinen, L
Citation: J. Uitto et L. Pulkkinen, Epidermolysis bullosa in Mexico, INT J DERM, 39(6), 2000, pp. 433-435
The gene gun: current applications in cutaneous gene therapy
Authors: Lin, MTS Pulkkinen, L Uitto, J Yoon, K
Citation: Mts. Lin et al., The gene gun: current applications in cutaneous gene therapy, INT J DERM, 39(3), 2000, pp. 161-170
Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplex
Authors: Morrell, DS Rubenstein, DS Briggaman, RA Fine, JD Pulkkinen, L Uitto, J
Citation: Ds. Morrell et al., Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplex, BR J DERM, 143(6), 2000, pp. 1342-1343
Splicing modulation of integrin beta 4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing
Authors: Chavanas, S Gache, Y Vailly, J Kanitakis, J Pulkkinen, L Uitto, J Ortonne, JP Meneguzzi, G
Citation: S. Chavanas et al., Splicing modulation of integrin beta 4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing, HUM MOL GEN, 8(11), 1999, pp. 2097-2105
Mutation analysis and molecular genetics of epidermolysis bullosa
Authors: Pulkkinen, L Uitto, J
Citation: L. Pulkkinen et J. Uitto, Mutation analysis and molecular genetics of epidermolysis bullosa, MATRIX BIOL, 18(1), 1999, pp. 29-42
Expression of plectin and HD1 epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophy
Authors: Shimizu, H Masunaga, T Kurihara, Y Owaribe, K Wiche, G Pulkkinen, L Uitto, J Nishikawa, T
Citation: H. Shimizu et al., Expression of plectin and HD1 epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophy, ARCH DERM R, 291(10), 1999, pp. 531-537
Emotion regulation strategies in relation to personality characteristics indicating low and high self-control of emotions
Authors: Kokkonen, M Pulkkinen, L
Citation: M. Kokkonen et L. Pulkkinen, Emotion regulation strategies in relation to personality characteristics indicating low and high self-control of emotions, PERS INDIV, 27(5), 1999, pp. 913-932
Epidermolysis bullosa simplex associated with muscular dystrophy: Phenotype-genotype correlations and review of the literature
Authors: Shimizu, H Takizawa, Y Pulkkinen, L Murata, S Kawai, M Hachisuka, H Udono, M Uitto, J Nishikawa, T
Citation: H. Shimizu et al., Epidermolysis bullosa simplex associated with muscular dystrophy: Phenotype-genotype correlations and review of the literature, J AM ACAD D, 41(6), 1999, pp. 950-956
The role of parents' self-esteem, mastery-orientation and social background in their parenting styles
Authors: Aunola, K Nurmi, JE Onatsu-Arvilommi, T Pulkkinen, L
Citation: K. Aunola et al., The role of parents' self-esteem, mastery-orientation and social background in their parenting styles, SC J PSYCHO, 40(4), 1999, pp. 307-317
Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosa
Authors: Pulkkinen, L Marinkovich, MP Tran, HT Lin, L Herron, GS Uitto, J
Citation: L. Pulkkinen et al., Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosa, J INVES DER, 113(6), 1999, pp. 1114-1118
Recurrent COL7A1 mutations in Japanese patients with dystrophic epidermolysis bullosa: Positional effects of premature termination codon mutations onclinical severity
Authors: Tamai, K Murai, T Mayama, M Kon, A Nomura, K Sawamura, D Hanada, K Hashimoto, I Shimizu, H Masunaga, T Nishikawa, T Mitsuhashi, Y Ishida-Yamamoto, A Ikeda, S Ogawa, H McGrath, JA Pulkkinen, L Uitto, J
Citation: K. Tamai et al., Recurrent COL7A1 mutations in Japanese patients with dystrophic epidermolysis bullosa: Positional effects of premature termination codon mutations onclinical severity, J INVES DER, 112(6), 1999, pp. 991-993
Dominant dystrophic epidermolysis bullosa (Pasini) caused by a novel glycine substitution mutation in the type VII collagen gene (COL7A1)
Authors: Jonkman, MF Moreno, G Rouan, F Oranje, AP Pulkkinen, L Uitto, J
Citation: Mf. Jonkman et al., Dominant dystrophic epidermolysis bullosa (Pasini) caused by a novel glycine substitution mutation in the type VII collagen gene (COL7A1), J INVES DER, 112(5), 1999, pp. 815-817
Four novel plectin gene mutations in Japanese patients with epidermolysis bullosa with muscular dystrophy disclosed by heteroduplex scanning and protein truncation tests
Authors: Takizawa, Y Shimizu, H Rouan, F Kawai, M Udono, M Pulkkinen, L Nishikawa, T Uitto, J
Citation: Y. Takizawa et al., Four novel plectin gene mutations in Japanese patients with epidermolysis bullosa with muscular dystrophy disclosed by heteroduplex scanning and protein truncation tests, J INVES DER, 112(1), 1999, pp. 109-112
Prenatal diagnosis of recessive dystrophic epidermolysis bullosa in a family at risk for recurrence by haplotype analysis of the type VII collagen gene
Authors: Bauer, JW Ortiz, S Hengstschlager, M Pulkkinen, L Uitto, J Hintner, H Rappersberger, K
Citation: Jw. Bauer et al., Prenatal diagnosis of recessive dystrophic epidermolysis bullosa in a family at risk for recurrence by haplotype analysis of the type VII collagen gene, HAUTARZT, 50(2), 1999, pp. 121-126
Personality antecedents of career orientation and stability among women compared to men
Authors: Pulkkinen, L Ohranen, M Tolvanen, A
Citation: L. Pulkkinen et al., Personality antecedents of career orientation and stability among women compared to men, J VOCAT BEH, 54(1), 1999, pp. 37-58
Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: Implications for geneticcounseling
Authors: Rouan, F Pulkkinen, L Jonkman, MF Bauer, JW Cserhalmi-Friedman, PB Christiano, AM Uitto, J
Citation: F. Rouan et al., Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: Implications for geneticcounseling, J INVES DER, 111(6), 1998, pp. 1210-1213
Novel premature termination codon mutations in the laminin gamma 2-chain gene (LAMC2) in Herlitz junctional epidermolysis bullosa
Authors: Takizawa, Y Shimizu, H Pulkkinen, L Nonaka, S Kubo, T Kado, Y Nishikawa, T Uitto, J
Citation: Y. Takizawa et al., Novel premature termination codon mutations in the laminin gamma 2-chain gene (LAMC2) in Herlitz junctional epidermolysis bullosa, J INVES DER, 111(6), 1998, pp. 1233-1234
Combination of a novel frameshift mutation (1929delCA) and a recurrent nonsense mutation (W610X) of the LAMB3 gene in a Japanese patient with Herlitzjunctional epidermolysis bullosa, and their application for prenatal testing
Authors: Takizawa, Y Shimizu, H Pulkkinen, L Suzumori, K Kakinuma, H Uitto, J Nishikawa, T
Citation: Y. Takizawa et al., Combination of a novel frameshift mutation (1929delCA) and a recurrent nonsense mutation (W610X) of the LAMB3 gene in a Japanese patient with Herlitzjunctional epidermolysis bullosa, and their application for prenatal testing, J INVES DER, 111(6), 1998, pp. 1239-1241
Heterozygosity for premature termination codon mutations in LAMB3 in siblings with non-lethal junctional epidermolysis
Authors: Pulkkinen, L Uitto, J
Citation: L. Pulkkinen et J. Uitto, Heterozygosity for premature termination codon mutations in LAMB3 in siblings with non-lethal junctional epidermolysis, J INVES DER, 111(6), 1998, pp. 1244-1246
Risultati: 1-25 | 26-50 | 51-51