Organification - AILBRY - Article Search

Results for 'Organification' :

Maternal-Fetal Transfer of Thyroxine in Congenital Hypothyroidism Due to a Total Organification Defect or Thyroid Agenesis

Publication Year: 1989

DOI: https://doi.org/10.1056/nejm198907063210103

Abstract:

Authors:
- Thomas Vulsma
- Margareth H. Gons
- Jan J. M. de Vijlder
Two Decades of Screening for Congenital Hypothyroidism in the Netherlands: TPO Gene Mutations in Total Iodide Organification Defects (an Update)

Publication Year: 2000

DOI: https://doi.org/10.1210/jcem.85.10.6878

Abstract:

Authors:
- Egbert Bakker
- Hennie Bikker
- Thomas Vulsma
- Janine S. E. de Randamie
- Brenda M. Wiedijk
- Jan J. M. de Vijlder
Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

Publication Year: 1996

DOI: https://doi.org/10.1038/ng0496-424

Abstract:

Authors:
- Val C. Sheffield
- Zaki Kraiem
- John C. Beck
- Darryl Nishimura
- Edwin M. Stone
- Muhamad Salameh
- O. Sadeh
- Benjamin Gläser
Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect

Publication Year: 2003

DOI: https://doi.org/10.1089/10507250360731550

Abstract:

Authors:
- Antonio C. Nascimento
- Dulce Rondina Guedes
- Cecilia S. Santos
- Meyer Knobel
- Ileana Gabriela Sanchez Rubio
- Geraldo Medeiros‐Neto
Molecular Analysis of Mutated Thyroid Peroxidase Detected in Patients with Total Iodide Organification Defects<sup>1</sup>

Publication Year: 1997

DOI: https://doi.org/10.1210/jcem.82.2.3729

Abstract:

Authors:
- Hennie Bikker
- Frank Baas
- Jan J. M. de Vijlder
Monoallelic Expression of Mutant Thyroid Peroxidase Allele Causing Total Iodide Organification Defect

Publication Year: 2003

DOI: https://doi.org/10.1210/jc.2002-021377

Abstract:

Authors:
- Laura Fugazzola
- Nadia Cerutti
- Deborah Mannavola
- Guia Vannucchi
- Claudia Fallini
- Luca Persani
- P. Beck‐Peccoz
Molecular Analysis of Mutated Thyroid Peroxidase Detected in Patients with Total Iodide Organification Defects

Publication Year: 1997

DOI: https://doi.org/10.1210/jc.82.2.649

Abstract:

Authors:
- Hennie Bikker
A novel mutation in the human thyroid peroxidase gene resulting in a total iodide organification defect

Publication Year: 1999

DOI: https://doi.org/10.1677/joe.0.1600267

Abstract:

Authors:
- Takuya Kotani
- Kazumi Umeki
- Ikuo Yamamoto
- Hatae Maesaka
- Kunihide Tachibana
- S Ohtaki
Transposition of the Thyroid Iodide Uptake and Organification System in Nonthyroid Tumor Cells by Adenoviral Vector-Mediated Gene Transfers

Publication Year: 2002

DOI: https://doi.org/10.1089/105072502753451922

Abstract:

Authors:
- Anne Boland
- Claire Magnon
- Sébastiano Filetti
- Jean-Michel Bidart
- Martin Schlumberger
- Patrice Yeh
- Michel Perricaudet
Defective Organification of Iodide Causing Hereditary Goitrous Hypothyroidism

Publication Year: 1993

DOI: https://doi.org/10.1089/thy.1993.3.143

Abstract:

Authors:
- Geraldo Medeiros‐Neto
- Ana Elisa C. Billerbeck
- B L Wajchenberg
- Héctor M. Targovnik
Clinical Description of Infants with Congenital Hypothyroidism and Iodide Organification Defects

Publication Year: 2008

DOI: https://doi.org/10.1159/000151597

Abstract:

Authors:
- Paolo Cavarzere
- Mireille Castanet
- Michel Polak
- M C Raux-Demay
- Sylvie Cabrol
- Jean‐Claude Carel
- Juliane Léger
- Paul Czernichow
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect

Publication Year: 1999

DOI: https://doi.org/10.1046/j.1365-2265.1999.00746.x

Abstract:

Authors:
- Cecília L. S. Santos
- Hennie Bikker
- Katia G. M. Rego
- Antonio C. Nascimento
- Marcos Antônio Tambascia
- Jan J. M. de Vijlder
- Geraldo Medeiros‐Neto
A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism.

Publication Year: 1994

DOI: https://doi.org/10.1210/jcem.79.1.8027236

Abstract:

Authors:
- Hennie Bikker
- Marcel T. den Hartog
- Frank Baas
- M. H. Gons
- T. Vulsma
- J J de Vijlder
Acute Effects of Propylthiouracil (PTU) on Thyroidal Iodide Organification and Peripheral Iodothyronine Deiodination: Correlation with Serum PTU Levels Measured by Radioimmunoassay*

Publication Year: 1982

DOI: https://doi.org/10.1210/jcem-54-1-101

Abstract:

Authors:
- David S. Cooper
- VELIA SAXE
- MICHAEL J. MESKELL
- Farahe Maloof
- E. Chester Ridgway
Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A&gt;C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect

Publication Year: 2005

DOI: https://doi.org/10.1373/clinchem.2005.058321

Abstract:

Authors:
- Viviana Varela
- Carina M. Rivolta
- Sebastián A. Esperante
- Laura Gruñeiro‐Papendieck
- Ana Chiesa
- Héctor M. Targovnik

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AILBRY - Article Search

Results for 'Organification' :

Maternal-Fetal Transfer of Thyroxine in Congenital Hypothyroidism Due to a Total Organification Defect or Thyroid Agenesis

Two Decades of Screening for Congenital Hypothyroidism in the Netherlands: TPO Gene Mutations in Total Iodide Organification Defects (an Update)

Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect

Molecular Analysis of Mutated Thyroid Peroxidase Detected in Patients with Total Iodide Organification Defects<sup>1</sup>

Monoallelic Expression of Mutant Thyroid Peroxidase Allele Causing Total Iodide Organification Defect

Molecular Analysis of Mutated Thyroid Peroxidase Detected in Patients with Total Iodide Organification Defects

A novel mutation in the human thyroid peroxidase gene resulting in a total iodide organification defect

Transposition of the Thyroid Iodide Uptake and Organification System in Nonthyroid Tumor Cells by Adenoviral Vector-Mediated Gene Transfers

Defective Organification of Iodide Causing Hereditary Goitrous Hypothyroidism

Clinical Description of Infants with Congenital Hypothyroidism and Iodide Organification Defects

A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect

A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism.

Acute Effects of Propylthiouracil (PTU) on Thyroidal Iodide Organification and Peripheral Iodothyronine Deiodination: Correlation with Serum PTU Levels Measured by Radioimmunoassay*

Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A&amp;gt;C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect

What is Boolean Searches

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Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect