15 documents found, page 1 of 2

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G46S PKU Mutation

Leandro, J; Simonsen, N; Tavares de Almeida, I; Leandro, P; Flatmark, T


The Human Phenylalanine Hydroxylase Protein

Leandro, P; Nascimento, C; Leandro, J; Violante, S; Ventura, F; Silva, MJ; Rivera, I; Tavares de Almeida, I


Co-expression of different subunits of human phenylalanine hydroxylase

Leandro, J; Nascimento, C; de Almeida, IT; Leandro, P

To study the interaction between two different subunits of the heteromeric human phenylalanine hydroxylase (hPAH), present in hyperphenylalaninemic (HPA) compound heterozygous patients, heteroallelic hPAH enzymes were produced. A dual vector expression sy


Functional characterization of heteromeric human phenylalanine hydroxylase prot...

Sequeira, AF; Leandro, J; Tavares de Almeida, I; Leandro, P

FCT (POCTI/MGI/40844/2001)


Heterozygote compound PKU patients

Leandro, P; Leandro, J; Tavares de Almeida, I

FCT: project POCTI/MGI/40844/2001



Biochemical characterization of chimerical mutant forms of human phenylalanine ...

Nascimento, C; Coelho, C; Leandro, J; de Almeida, IT; Leandro, P


Osteomielite da base do crâneo: breve revisão a propósito de um caso clínico

Freire, F; Adónis, C; Caratão, J; Leandro, J; Veiga, G

Os autores opresentom o caso clínico de um doente diabético com otite externa moligna complicada por osteomielite do base do crânio, com atingimento de vários nervos cranianos e que culminou na morfe do doente. Esfe caso serve de introdução o uma revisão sobre os aspectos mais relevantes e actuais relacionados com a abordagem desta patologia que, nos dias de hoje, e mesmo com a possibilidade de recurso a vários...


Co-expression of two different mutant alleles of phenylalanine hydroxylase gene...

Leandro, J; Nascimento, C; Tavares de Almeida, I; Leandro, P


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