IngentaConnect Search Results

Membranoproliferative Glomerulonephritis Associated with Psoriasis Vulgaris

Authors: Akoglu, Hadim; Dede, Fatih; Akoglu, Gulsen; Gonul, Ipek Isık; Odabas, Ali Rıza

Source: Renal Failure, Volume 31, Number 9, October 2009 , pp. 858-861(4)

Molecular Diagnosis of PMP22 Gene Duplications and Deletions: Comparison of Different Methods

Authors: Stangler Herodež, .; Zagradišnik, B.; Erjavec Škerget, A.; Zagorac, A.; Kokalj Vokač, N.

Source: The Journal of International Medical Research, Volume 37, Number 5, September 2009 , pp. 1626-1631(6)

Unexpected clinical involvement of hereditary total leuconychia with congenital fibrosis of the extraocular muscles in three generations

Authors: Karadeniz, N.; Erkek, E.; Taner, P.

Source: Clinical & Experimental Dermatology, Volume 34, Number 8, December 2009 , pp. e570-e572(1)

Publisher: Blackwell Publishing

Two Taiwanese siblings with dyschromatosis universalis hereditaria

Authors: Wu, C. Y.; Huang, W. H.

Source: Clinical & Experimental Dermatology, Volume 34, Number 8, December 2009 , pp. e666-e669(1)

Publisher: Blackwell Publishing

Malformations of the index nails

Authors: Hussein, T. P.; Brandt, H. R. C.; Gabbi, T. V. B.; Nico, M. M. S.

Source: Clinical & Experimental Dermatology, Volume 34, Number 8, December 2009 , pp. 890-891(2)

Publisher: Blackwell Publishing

Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis

Authors: Düzenli, S.; Redler, S.; Müller, M.; Polat, M.; Dogruer, D.; Pasternack, S. M.; Betz, R. C.

Source: Clinical & Experimental Dermatology, Volume 34, Number 8, December 2009 , pp. e953-e956(1)

Publisher: Blackwell Publishing

Phenotype and genotype in females with POU3F4 mutations

Authors: Marlin, S; Moizard, MP; David, A; Chaissang, N; Raynaud, M; Jonard, L; Feldmann, D; Loundon, N; Denoyelle, F; Toutain, A

Source: Clinical Genetics, Volume 76, Number 6, December 2009 , pp. 558-563(6)

Publisher: Blackwell Publishing

Thirty Years of Research into Rendu-Osler-Weber Disease in France: Historical Demography, Population Genetics and Molecular Biology

Authors: Brunet, Guy; Lesca, Gaëtan; Génin, Emmanuelle; Dupuis-Girod, Sophie; Bideau, Alain; Plauchu, Henri

Source: Population, Volume 64, Number 2, 2009 , pp. 273-291(19)

Publisher: INED - Institut national d'études démographiques

Receptor for activated C-kinase 1 regulates the cellular localization and function of ABCB4

Authors: Ikebuchi, Yuki; Takada, Tappei; Ito, Kousei; Yoshikado, Takashi; Anzai, Naohiko; Kanai, Yoshikatsu; Suzuki, Hiroshi

Source: Hepatology Research, Volume 39, Number 11, November 2009 , pp. 1091-1107(17)

Publisher: Blackwell Publishing

Ethical, legal and social implications of prenatal and preimplantation genetic testing for cancer susceptibility

Authors: Wang, C-W.; Hui, E.C.

Source: Reproductive BioMedicine Online, Volume 19, Supplement 2, November 2009 , pp. 23-33(11)

Publisher: Reproductive Healthcare Ltd

Cardiac transplantation should be considered in selected patients with either AL or hereditary forms of amyloidosis: the UK National Amyloidosis Centre experience

Source: Internal Medicine Journal, Volume 39, Number 11, November 2009 , pp. 786-787(2)

Publisher: Blackwell Publishing

New developments in the regulation of intestinal copper absorption

Authors: van den Berghe, Peter VE; Klomp, Leo WJ

Source: Nutrition Reviews, Volume 67, Number 11, November 2009 , pp. 658-672(15)

Publisher: Blackwell Publishing

Looks and Living Kinds: Varieties of Racial Cognition in Bahia, Brazil

Author: Jones, Doug

Source: Journal of Cognition and Culture, Volume 9, Number 3, 2009 , pp. 247-269(23)

Publisher: BRILL

Whole-genome scan for guttural pouch tympany in Arabian and German warmblood horses

Authors: Zeitz, A.; Spötter, A.; Blazyczek, I.; Diesterbeck, U.; Ohnesorge, B.; Deegen, E.; Distl, O.

Source: Animal Genetics, Volume 40, Number 6, December 2009 , pp. 917-924(8)

Publisher: Blackwell Publishing

Human C1-Esterase Inhibitor Concentrate (Berinert®)

Author: Keating, Gillian M.

Source: BioDrugs, Volume 23, Number 6, 1 December 2009 , pp. 399-406(8)

Publisher: Adis International

Diagnosis of mild platelet function disorders. Reliability and usefulness of light transmission platelet aggregation and serotonin secretion assays

Authors: Quiroga, Teresa; Goycoolea, Manuela; Matus, Valeria; Zúñiga, Pamela; Martínez, Carlos; Garrido, Marcelo; Aranda, Eduardo; Leighton, Federico; Panes, Olga; Pereira, Jaime; Mezzano, Diego

Source: British Journal of Haematology, Volume 147, Number 5, December 2009 , pp. 729-736(8)

Publisher: Blackwell Publishing

Does Oxidative Stress Modulate Left Ventricular Diastolic Function in Asymptomatic Subjects with Hereditary Hemochromatosis?

Authors: Shizukuda, Yukitaka; Bolan, Charles D.; Tripodi, Dorothy J.; Sachdev, Vandana; Nguyen, Tammy T.; Botello, Gilberto; Yau, Yu-Ying; Sidenko, Stanislav; Inez, Ernst; Ali, Mir I.; Waclawiw, Myron A.; Leitman, Susan F.; Rosing, Douglas R.

Source: Echocardiography - Jnl Cardiovascular Ultrasound & Allied Techniques, Volume 26, Number 10, November 2009 , pp. 1153-1158(6)

Publisher: Blackwell Publishing

Neonatal thrombo-embolism: risk factors, clinical features and outcome

Authors: Demirel, N.; Aydin, M.; Zenciroglu, A.; Bas, A.Y.; Yarali, N.; Okumus, N.; Cinar, G.; Ipek, M.S.

Source: Annals of Tropical Paediatrics: International Child Health, Volume 29, Number 4, December 2009 , pp. 271-279(9)

Publisher: Maney Publishing

Risk of colorectal neoplasia associated with the adenomatous polyposis coli E1317Q variant

Authors: Hall, M. J.; Liberman, E.; Dulkart, O.; Galazan, L.; Sagiv, E.; Shmueli, E.; Kazanov, D.; Hallak, A.; Moshkowitz, M.; Figer, A.; Kraus, S.; Inbar, M.; Neugut, A. I.; Arber, N.

Source: Annals of Oncology, Volume 20, Number 9, 24 September 2009 , pp. 1517-1521(5)

Publisher: Oxford University Press

Hereditary congenital hypopigmented and hyperpigmented macules (Westerhof syndrome) in two siblings

Authors: Vélez, A.; Salido, R.; Amorrich-Campos, V.; Garnacho-Saucedo, G.; Alvarez-López, M.A.; Galán, M.; Moreno-Giménez, J.C.

Source: British Journal of Dermatology, Volume 161, Number 6, December 2009 , pp. 1399-1400(2)

Publisher: Blackwell Publishing