Rabson-Mendenhall syndrome with recurrent cerebral infarcts caused by a novel INSR mutation.

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Successful rhIGF1 treatment for over 5 years in a patient with severe insulin resistance due to homozygous insulin receptor mutation.Rabson Mendenhall Syndrome caused by a novel missense mutation.

P2860

Q36573050-0E7826F5-DE2B-4898-9311-A14022E71BF3 Q41855816-89B1D75B-5FC5-4917-B20A-C75504851805

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Rabson-Mendenhall syndrome with recurrent cerebral infarcts caused by a novel INSR mutation.

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http://www.wikidata.org/entity/Q51278319

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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name

Rabson-Mendenhall syndrome wit ...... used by a novel INSR mutation.

@en

Rabson-Mendenhall syndrome wit ...... used by a novel INSR mutation.

@nl

type

Item

label

Rabson-Mendenhall syndrome wit ...... used by a novel INSR mutation.

@en

Rabson-Mendenhall syndrome wit ...... used by a novel INSR mutation.

@nl

prefLabel

Rabson-Mendenhall syndrome wit ...... used by a novel INSR mutation.

@en

Rabson-Mendenhall syndrome wit ...... used by a novel INSR mutation.

@nl

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Rabson-Mendenhall syndrome wit ...... used by a novel INSR mutation.

@en

P2093

Saritha Mohanan

http://www.w3.org/2001/XMLSchema#string

Sivaranjini Ramassamy

http://www.w3.org/2001/XMLSchema#string

Vir S Negi

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P2860

Efficacy of recombinant methionyl human leptin therapy for the extreme insulin resistance of the Rabson-Mendenhall syndrome

Genetic Syndromes of Severe Insulin Resistance

Multidrug therapy in a patient with Rabson–Mendenhall syndrome

Genotype-phenotype correlation in inherited severe insulin resistance.

Five mutant alleles of the insulin receptor gene in patients with genetic forms of insulin resistance.

Founder effect in the Horn of Africa for an insulin receptor mutation that may impair receptor recycling

Genes, growth factors and acanthosis nigricans.

Excess insulin binding to insulin-like growth factor receptors: proposed mechanism for acanthosis nigricans.

Rabson-Mendenhall syndrome: two case reports and a brief review of the literature.

An in-frame insertion in exon 3 and a nonsense mutation in exon 2 of the insulin receptor gene associated with severe insulin resistance in a patient with Rabson-Mendenhall syndrome.

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182-185

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scholarly article

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10.1111/J.1365-4632.2012.05665.X

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http://www.w3.org/2001/XMLSchema#string

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http://www.w3.org/2001/XMLSchema#string

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Robert K Semple

Devinder M. Thappa

Narayanan Parameswaran

Laxmisha Chandrashekar

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2013-02-01T00:00:00Z

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P698

23347304

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Rabson-Mendenhall syndrome with recurrent cerebral infarcts caused by a novel INSR mutation.

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P2860

P2860

Rabson-Mendenhall syndrome with recurrent cerebral infarcts caused by a novel INSR mutation.

description

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P1433

P1476

P2093

P2860

P304

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P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698