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Stigmatization, culture and counseling a commentary on growing up and living wi…

Gaff(CL),Clarke(A) J Genet Couns 2007-10-00

...NF1) is unusual in its detail of one woman's account of others' interactions with her and the impact on her life. It rai...

[Juvenile myelomonocytic leukaemia, xanthoma, and neurofibromatosis type 1].

Benessahraoui(M),Aubin(F),Paratte(F),Plouvie… Arch Pediatr 2003-10-00

...NF1 in a young child should alert to a possible development of JMML, especially in patients with a family history of NF1...

Loss of SDHB and NF1 genes in a malignant phyllodes tumor of the breast as dete…

Lee(J),Wang(J),Torbenson(M),Lu(Y),Liu(QZ),Li… Cancer Genet Cytogenet 2010-01-15

...NF1). Both genes are associated with hereditary cancer syndromes, including gastrointestinal stromal tumors. Whether the...

Dopamine deficiency underlies learning deficits in neurofibromatosis-1 mice.

Diggs-Andrews(KA),Tokuda(K),Izumi(Y),Zorumsk… Ann Neurol 2013-02-00

Children with neurofibromatosis type 1 (NF1) are prone to learning and behavioral abnormalities, including problems with...

Malignant Peripheral Nerve Sheath Tumour: CT and MRI Findings.

Sperandio(M),Di Poce(I),Ricci(A),Di Trapano(… Case Rep Radiol 2013-00-00

...NF1). In the literature five cases of MPNST arising from the parapharyngeal space (PPS) in patients without neurofibroma...

Role of maxillofacial surgery in patients with neurofibromatosis type I.

Fadda(MT),Giustini(SS),Verdino(GG),Bartoli(D… J Craniofac Surg 2007-05-00

Neurofibromas are a clinical manifestation of neurofibromatos is type I (NF1). Management of these tumors remains a chal...

Lisch nodules of the iris in neurofibromatosis type 1.

Richetta(A),Giustini(S),Recupero(SM),Pezza(M… J Eur Acad Dermatol Venereol 2004-05-00

...NF1) is a common autosomal dominant disease. The Lisch nodule represents one of the most common NF1 ocular manifestation...

[Ophthalmological manifestations of Von Recklinghausen disease].

Benchekroun(O),Lamari(H),Moutawakkil(A),Laou… J Fr Ophtalmol 1997-00-00

To evaluate the frequency of Von Recklinghausen neurofibromatosis type 1 (NF1) ocular abnormalities. A retrospective stu...

Generation of KCL024 research grade human embryonic stem cell line carrying a m…

Hewitson(Heema),Wood(Victoria),Kadeva(Neli),… Stem Cell Res 0000-00-00

...NF1 gene encoding neurofibromin (c.3739-3742 ∆TTTG). Mutations in this gene have been linked to neurofibromatosis type 1...

Generation of KCL025 research grade human embryonic stem cell line carrying a m…

Hewitson(Heema),Wood(Victoria),Kadeva(Neli),… Stem Cell Res 0000-00-00

...NF1 gene encoding neurofibromin (c.3739-3742 ΔTTTG). Mutations in this gene have been linked to neurofibromatosis type 1...

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