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Material Type: Artigo
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11 beta-hydroxysteroid-dehydrogenase: characteristics and the clinical significance of a key enzyme in cortisol metabolismKerstens, M N ; Dullaart, R PNederlands tijdschrift voor geneeskunde, 1999-03, Vol.143 (10), p.509-514NetherlandsTexto completo disponível |
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Material Type: Artigo
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11-β hydroxysteroid type 1 knockout mice display an antidepressant-like phenotype in the forced swim testSlattery, David A. ; Uzunov, Doncho P. ; Cryan, John F.Acta neuropsychiatrica, 2016-02, Vol.28 (1), p.55-60 [Periódico revisado por pares]Cambridge, UK: Cambridge University PressTexto completo disponível |
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Material Type: Artigo
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16S rRNA sequence analysis: application and pitfallsvan Hattem, Jarne M ; de Wever, BobNederlands tijdschrift voor geneeskunde, 2019-10, Vol.163NetherlandsTexto completo disponível |
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Material Type: Artigo
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1949-1989: glucocorticoids, their receptors and variable clinical responsevan Hal, P T ; Mulder, E ; Hoogsteden, H C ; Hilvering, CNederlands tijdschrift voor geneeskunde, 1989-07, Vol.133 (26), p.1305-1310NetherlandsTexto completo disponível |
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Material Type: Artigo
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2 families with malignant atrophic papulosis (Degos disease)Beljaards, R C ; Starink, T M ; Meuwissen, S GNederlands tijdschrift voor geneeskunde, 1988-02, Vol.132 (6), p.269-271NetherlandsTexto completo disponível |
6 |
Material Type: Artigo
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2 families with meningococcal infection and a hereditary disorder of the 5th component of the complement systemFijen, C A ; Kuijper, E J ; Lindeboom, S F ; van Os, J ; van Putten, J PNederlands tijdschrift voor geneeskunde, 1989-09, Vol.133 (36), p.1796NetherlandsTexto completo disponível |
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Material Type: Artigo
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2 patients with autosomal recessive generalized myotoniaFrijns, C J ; Wouda, E J ; Linssen, W H ; Snijders, C JNederlands tijdschrift voor geneeskunde, 1994-04, Vol.138 (14), p.726-728NetherlandsTexto completo disponível |
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Material Type: Artigo
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22q11.2 deletion syndrome diagnosed in an adult maleHassing, Robert-Jan ; Verhagen, Judith M A ; van de Laar, Ingrid M B H ; van Daele, Paul L ANederlands tijdschrift voor geneeskunde, 2011, Vol.155 (40), p.A3644NetherlandsTexto completo disponível |
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Material Type: Artigo
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3 children with velocardiofacial (Shprintzen) syndromeLie, D A ; Beemer, F ANederlands tijdschrift voor geneeskunde, 1996-02, Vol.140 (7), p.372-375NetherlandsTexto completo disponível |
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Material Type: Artigo
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3 examples of fetal genetic neuromuscular disorders which lead to hydramnionTeeuw, A H ; Barth, P G ; van Sonderen, L ; Zondervan, H ANederlands tijdschrift voor geneeskunde, 1993-05, Vol.137 (18), p.908-913NetherlandsTexto completo disponível |