Update Review and Clinical Presentation in Congenital Insensitivity to Pain and Anhidrosis.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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Update Review and Clinical Pre ...... tivity to Pain and Anhidrosis.

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Update Review and Clinical Pre ...... tivity to Pain and Anhidrosis.

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Update Review and Clinical Pre ...... tivity to Pain and Anhidrosis.

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Update Review and Clinical Pre ...... tivity to Pain and Anhidrosis.

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Update Review and Clinical Pre ...... tivity to Pain and Anhidrosis.

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Update Review and Clinical Pre ...... tivity to Pain and Anhidrosis.

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Update Review and Clinical Pre ...... tivity to Pain and Anhidrosis.

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D Gutiérrez-de la Iglesia

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G Knörr-Giménez

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M Cabrera-González

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S Ricart

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P2860

Structure and organization of the human TRKA gene encoding a high affinity receptor for nerve growth factor

Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve g

Oral and craniofacial manifestations and two novel missense mutations of the NTRK1 gene identified in the patient with congenital insensitivity to pain with anhidrosis

Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor.

Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.

An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis.

Congenital insensitivity to pain with anhydrosis. A unique syndrome in two male siblings.

Indolent corneal ulcers in a patient with congenital insensitivity to pain with anhidrosis: a case report and literature review.

Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis.

Rapid physical mapping of the human trk protooncogene (NTRK1) to human chromosome 1q21-q22 by P1 clone selection, fluorescence in situ hybridization (FISH), and computer-assisted microscopy.

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10.1155/2015/589852

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2015

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Laura Montessarat Pérez-López

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2015-10-22T00:00:00Z

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birth defect

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