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Health supervision for children with neurofibromatosis type 1
Neuroibromatosis type 1 (NF1) is a multisystem disorder that primarily involves the skin and
peripheral nervous system. Its population prevalence is approximately 1 in 3000. The …
peripheral nervous system. Its population prevalence is approximately 1 in 3000. The …
Neurofibromatosis type 1: a multidisciplinary approach to care
Neurofibromatosis type 1 is a relatively common inherited disorder. Patients have a high
predisposition to develop both benign and malignant tumours. Although many …
predisposition to develop both benign and malignant tumours. Although many …
Comparison of cancer prevalence in patients with neurofibromatosis type 1 at an academic cancer center vs in the general population from 1985 to 2020
Importance Neurofibromatosis type 1 (NF1) is a complex genetic disorder that is associated
with not only neurofibromas, but also an increased susceptibility to other neoplasms …
with not only neurofibromas, but also an increased susceptibility to other neoplasms …
A RASopathy gene commonly mutated in cancer: the neurofibromatosis type 1 tumour suppressor
Abstract Neurofibromatosis type 1 (NF1) is a common genetic disorder that predisposes
affected individuals to tumours. The NF1 gene encodes a RAS GTPase-activating protein …
affected individuals to tumours. The NF1 gene encodes a RAS GTPase-activating protein …
Neurofibromatosis 1 French national guidelines based on an extensive literature review since 1966
Neurofibromatosis type 1 is a relatively common genetic disease, with a prevalence ranging
between 1/3000 and 1/6000 people worldwide. The disease affects multiple systems with …
between 1/3000 and 1/6000 people worldwide. The disease affects multiple systems with …
Guidelines for the diagnosis and management of individuals with neurofibromatosis 1
Neurofibromatosis 1 (NF1) is a common neurocutaneous condition with an autosomal
dominant pattern of inheritance. The complications are diverse and disease expression …
dominant pattern of inheritance. The complications are diverse and disease expression …
[کتاب][B] Moss & Adams' heart disease in infants, children, and adolescents: including the fetus and young adult
HD Allen, DJ Driscoll, RE Shaddy, TF Feltes - 2013 - books.google.com
This 8th Edition of Moss and Adams' Heart Disease in Infants, Children, and Adolescents:
Including the Fetus and Young Adult, provides updated and useful information from leading …
Including the Fetus and Young Adult, provides updated and useful information from leading …
Lessons on the pathogenesis of aneurysm from heritable conditions
Aortic aneurysm is common, accounting for 1–2% of all deaths in industrialized countries.
Early theories of the causes of human aneurysm mostly focused on inherited or acquired …
Early theories of the causes of human aneurysm mostly focused on inherited or acquired …
Neurofibromatosis type 1 revisited
Neurofibromatosis type 1 (NF1) is an autosomal dominant condition with a worldwide
incidence of∼ 1 per 2500 to 3000 individuals. Caused by a germ-line–inactivating mutation …
incidence of∼ 1 per 2500 to 3000 individuals. Caused by a germ-line–inactivating mutation …
[HTML][HTML] Clinical and genetic aspects of neurofibromatosis 1
Neurofibromatosis 1 is an autosomal dominant disorder characterized by multiple café-au-
lait spots, axillary and inguinal freckling, multiple cutaneous neurofibromas, and iris Lisch …
lait spots, axillary and inguinal freckling, multiple cutaneous neurofibromas, and iris Lisch …