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T Rohrer Selected Research

furimidazoline

11/2012HDR syndrome: a follow-up genotype-phenotype analysis of a de novo missense Thr272Ile mutation in exon 4 of GATA3.

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T Rohrer Research Topics

Disease

2Infections
06/2014 - 01/2009
1Bronchitis
07/2015
1Crohn Disease (Crohn's Disease)
07/2015
1Barakat syndrome
11/2012
1Bilateral Hearing Loss
11/2012
1Deafness (Deaf Mutism)
11/2012
1Hypoparathyroidism
11/2012
1Subdural Hematoma (Subdural Hemorrhage)
10/2009
1Hemorrhage
10/2009
1Wounds and Injuries (Trauma)
10/2009
1Shaken Baby Syndrome
10/2009
1Hematoma
10/2009
1Silver-Russell Syndrome
01/2009
1Congenital Heart Defects (Congenital Heart Defect)
01/2009
1Hyperthyroidism
06/2002
1Goiter
06/2002
1Attention Deficit Disorder with Hyperactivity (Attention Deficit Hyperactivity Disorder)
06/2002
1Neoplasms (Cancer)
03/2001

Drug/Important Bio-Agent (IBA)

1Infliximab (Remicade)FDA Link
07/2015
1Transcription Factors (Transcription Factor)IBA
11/2012
1furimidazolineIBA
11/2012
1Retinaldehyde (Retinal)IBA
10/2009
1Thyroid HormonesIBA
06/2002
1Thyrotropin (Thyroid-Stimulating Hormone)FDA Link
06/2002

Therapy/Procedure

1Transplantation
06/2014
1Hearing Aids (Hearing Aid)
11/2012
1Traction
10/2009
1Therapeutics
01/2009
1Mohs Surgery (Mohs' Micrographic Surgery)
03/2001