Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin.

Mitogen accumulation in von Recklinghausen neurofibromatosis.

DNA deletion in patients with von Recklinghausen neurofibromatosis.

Von Recklinghausen disease (neurofibromatosis type 1): beyond skin involvement.

Vasculopathies of Neurofibromatosis Type 1 (von Recklinghausen Disease).

Ehlers-Danlos syndrome combined with von Recklinghausen neurofibromatosis.

Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.

Abnormal regulation of mammalian p21ras contributes to malignant tumor growth in von Recklinghausen (type 1) neurofibromatosis.

Malignant peripheral nerve sheath tumor (malignant schwannoma) of urinary bladder in von Recklinghausen neurofibromatosis.

The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations.

Genetic and physical map of the von Recklinghausen neurofibromatosis (NF1) region on chromosome 17.

Diagnosis: Von Recklinghausen disease (NF1).

[Lisch nodules in Von Recklinghausen disease].

neurofibromatosis.

Von recklinghausen disease: one patient - various problems.

Virchow's triad: Kussmaul, Quincke and von Recklinghausen.

Cervical neurofibroma and generalised spinal stenosis in von Recklinghausen disease.

[Consanguineous marriage and morbi-mortality, short literature review based on an exceptional association: Usher syndrome and Von Recklinghausen neurofibromatosis].

[Orthopedic manifestations of neurofibromatosis type 1 or Recklinghausen disease].

[Von Recklinghausen disease complicated with head and neck plexiform neurofibromas].

Von Hippel's disease in association with von Recklinghausen's neurofibromatosis.

[Small bowel stromal tumor associated with von Recklinghausen disease].

von Recklinghausen neurofibroma produces neuronal and glial growth-modulating factors.

Esophageal achalasia associated with von Recklinghausen's neurofibromatosis.

Suggest Documents

The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin.

Mitogen accumulation in von Recklinghausen neurofibromatosis.

DNA deletion in patients with von Recklinghausen neurofibromatosis.

Von Recklinghausen disease (neurofibromatosis type 1): beyond skin involvement.

Vasculopathies of Neurofibromatosis Type 1 (von Recklinghausen Disease).

Ehlers-Danlos syndrome combined with von Recklinghausen neurofibromatosis.

Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.

Abnormal regulation of mammalian p21ras contributes to malignant tumor growth in von Recklinghausen (type 1) neurofibromatosis.

Malignant peripheral nerve sheath tumor (malignant schwannoma) of urinary bladder in von Recklinghausen neurofibromatosis.

The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations.

Genetic and physical map of the von Recklinghausen neurofibromatosis (NF1) region on chromosome 17.

Diagnosis: Von Recklinghausen disease (NF1).

[Lisch nodules in Von Recklinghausen disease].

neurofibromatosis.

Von recklinghausen disease: one patient - various problems.

Virchow's triad: Kussmaul, Quincke and von Recklinghausen.

Cervical neurofibroma and generalised spinal stenosis in von Recklinghausen disease.

[Consanguineous marriage and morbi-mortality, short literature review based on an exceptional association: Usher syndrome and Von Recklinghausen neurofibromatosis].

[Orthopedic manifestations of neurofibromatosis type 1 or Recklinghausen disease].

[Von Recklinghausen disease complicated with head and neck plexiform neurofibromas].

Von Hippel's disease in association with von Recklinghausen's neurofibromatosis.

[Small bowel stromal tumor associated with von Recklinghausen disease].

von Recklinghausen neurofibroma produces neuronal and glial growth-modulating factors.

Esophageal achalasia associated with von Recklinghausen's neurofibromatosis.

Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

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