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Mostrando 941 - 960 Resultados de 1,643 Para Buscar '"Café"', tiempo de consulta: 0.31s Limitar resultados
  1. 941
    “…Neurofibromatosis type 1 (NF1) is one of the most common neurocutaneous genetic disorders, presenting with different cutaneous features such as café-au-lait macules, intertriginous skin freckling, and neurofibromas. …”
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    Insights into the Pathogenesis of NF1-Associated Neoplasms
  2. 942
    “…Classic form includes triad of fibrous dysplasia, café au late spots and autonomous hyper function of one or more endocrine pathways. …”
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    A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
  3. 943
    “…BACKGROUND: McCune–Albright syndrome (MAS) is a rare heterogeneous genetic disorder that is characterized by a triad of polyostotic fibrous dysplasia (FD), café au lait spots (CAL), and multiple hyperfunctional endocrinopathies. …”
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    Delayed Diagnosis of McCune–Albright Syndrome
  4. 944
    “…Neurofibromatosis type 1 (NF1) (von Recklinghausen’s disease) is an autosomal dominant disorder characterized by café-au-lait spots, pigmented hamartomas of the iris, and multiple neurofibromas. …”
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    Spontaneous Near Fatal Hemorrhage into Neurofibromatosis Type 1 Lesion in the Scalp
  5. 945
    “…McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. …”
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    A case report of McCune–Albright syndrome with hepatic manifestations
  6. 946
    “…On examination, he had café au lait spots and central hypotonia. MRI brain with contrast revealed bilateral bulky enhancing optic nerves with involvement of chiasma. …”
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    Optic Nerve Glioma in Neurofibromatosis: Radiological Clues to Diagnosis in a Young Child
  7. 947
    “…Neurofibromatosis type 1 (NF1) is an autosomal dominant condition characterized by café-au-lait spots, cutaneous neurofibromas, axillary and inguinal freckling, and iris Lisch nodules; however, the presentations vary greatly, even within families. …”
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    A Rare Case of Neuroendocrine Tumor in a Patient With Neurofibromatosis Type 1: Is There Any Association?
  8. 948
    por Palm, Jenny, Ambrose, Aimee
    Publicado 2023
    “…RESULTS: The article presents four different events: (1) a physical walk to an energy recovery facility, (2) a walk to view a building’s heat exchanger, (3) a round-table discussion using pictures to communicate in a language café, and (4) a virtual tour around an Energy Recovery Facility. …”
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    Exploring energy citizenship in the urban heating system with the ‘Walking with Energy’ methodology
  9. 949
    “…It is characterized by the classical triad of polyostotic fibrous dysplasia, café-au-lait skin spots and peripheral precocious puberty (PPP). …”
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    MON-247 Clinical Characterization of Female Peripheral Precocious Puberty Due to McCune-Albright Syndrome
  10. 950
    “…Background: McCune-Albright syndrome (MAS) is a well described genetic syndrome characterized by café-au-lait spots, polyostotic fibrous dysplasia, and hyperfunctioning endocrinopathies. …”
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    SUN-476 Risk of Thyroid Cancer in McCune-Albright Syndrome
  11. 951
    “…We offered an inclusive café that was open for extended hours as a place to socialize and a center for activities that included monthly public lectures. …”
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    Promoting cultural change towards dementia friendly communities: a multi-level intervention in Japan
  12. 952
    “…Cutaneous schwannomas are the most frequent but are often underdiagnosed. Café au lait macules are frequent, but atypical and mostly in small numbers. …”
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    Dermatologic manifestations in paediatric neurofibromatosis type 2: a cross sectional descriptive multicentric study
  13. 953
    “…Participatory methodologies were carried out: 1) semi-structured interviews with department heads (N = 12, 60%); 2) world cafe workshops open to a group of workers (N = 63, 37%); 3) a Quick and Colorful voting session open to a group of workers (N = 108, 63%); and 4) Hanlon matrix with 19 actions to be prioritized (N = 12 services, 60%). …”
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    Tackling health inequalities in a public health organization: the case of the Barcelona Public Health Agency
  14. 954
    Publicado 2002
    Video VHS
    Die Ehe der Maria Braun The Marriage of Maria Braun /
  15. 955
    por González Alafita, Rita
    Publicado 1988
    Tabla de Contenidos: “…De la farmacia al templo espiritista -- De la leña al gas y de la jícara al vaso de peltre -- Del trapiche a la purería, y de ésta al "jabón negro" pasando por el café, hasta aparecer los emigrantes -- El devenir educativo de los olutecos -- Lucha de los campesinos por la tierra -- Religión y fiesta en Oluta -- Los rituales fúnebres -- Las danzas de nuestro pueblo -- La danza de la conquista -- La danza de los arrieros y morenos -- La danza de la zandunga -- La danza del chenu ...…”
    Libro
    Oluta : apuntes para su historia
  16. 956
    Tabla de Contenidos: “…Los inicios del cultivo de café en Soconusco y la inmigración extranjera / Daniela Spencer -- Empresas y fincas cafetaleras en la década de 1910-1920 -- Las empresas alemanas e general / Brígida von Mentz -- Soconusco en la revolución / Daniela Spencer -- Economía y movimiento laboral en las fincas cafetaleras de Soconusco ... -- v. 2. …”
    Libro
    Los empresarios alemanes, el Tercer Reich y la oposición de derecha a Cárdenas
  17. 957
    “…The patients with generalized form of NF1 are characterized by multiple café-au-lait spots and neurofibromas and diagnosed easily. …”
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    SEGMENTAL NEUROFIBROMATOSIS: A REPORT OF 3 CASES
  18. 958
    “…Neurofibromatosis-1 (NF-1) is a relatively common autosomal dominant disease characterized by multiple cutaneous fibromatoses and café au lait spots. It is associated with the mutation of NF-1 gene, a tumor suppressor gene located on chromosome 17q11.2. …”
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    Intraoral presentation of multiple malignant peripheral nerve sheath tumors associated with neurofibromatosis-1
  19. 959
    “…Typical clinical manifestations of neurofibromatosis are cafe-au-lait spots and multiple cutaneous tumors. …”
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    Imaging Review of Neurofibromatosis: Helpful Aspects for Early Detection
  20. 960
    “…Turcot syndrome is an autosomal recessive disorder clinically characterized by the occurrence of primary tumors of the central nervous system and adenomatous colonic polyps during the first or second decades of life, with a spectrum of clinical features such as “café-au-lait” spots, axillary freckling, and hyperpigmented spots. …”
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    First Case Report of Turcot Syndrome Type 1 in Colombia
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