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Cellular and Molecular Pathways Leading to External Root Resorption

Journal of Dental Research, 2017-02, Vol.96 (2), p.145-152

2017

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The Use of Small Titanium Screws for Orthodontic Anchorage

Journal of dental research, 2003-05, Vol.82 (5), p.377-381

2003

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Genetic and treatment-related risk factors associated with external apical root resorption (EARR) concurrent with orthodontia

Orthodontics & craniofacial research, 2015-04, Vol.18 (S1), p.71-82

2015

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Accuracy of mandibular proximal segment position using virtual surgical planning and custom osteosynthesis plates

International journal of oral and maxillofacial surgery, 2022-02, Vol.51 (2), p.219-225

2022

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Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia)

Orthodontics & craniofacial research, 2007-08, Vol.10 (3), p.121-128

Hartsfield, JK

2007

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Pathways in external apical root resorption associated with orthodontia

Orthodontics & craniofacial research, 2009-08, Vol.12 (3), p.236-242

Hartsfield Jr, JK

2009

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In vitro evaluation of osteoblast responses to carbon nanotube-coated titanium surfaces

Progress in orthodontics, 2016-12, Vol.17 (1), p.23-9, Article 23

2016

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Exclusion of Class III Malocclusion Candidate Loci in Brazilian Families

Journal of dental research, 2011-10, Vol.90 (10), p.1202-1205

2011

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Comparison of reliability in anatomical landmark identification using two-dimensional digital cephalometrics and three-dimensional cone beam computed tomography in vivo

Dento-maxillo-facial radiology, 2009-07, Vol.38 (5), p.262-273

2009

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Genetic Predisposition to External Apical Root Resorption in Orthodontic Patients: Linkage of Chromosome-18 Marker

Journal of dental research, 2003-05, Vol.82 (5), p.356-360

2003

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De novo 10q22 interstitial deletion

Journal of medical genetics, 1999-01, Vol.36 (1), p.71-72

1999

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A novel FGFR2 gene mutation in Crouzon syndrome associated with apparent nonpenetrance

The Cleft palate-craniofacial journal, 1999-11, Vol.36 (6), p.533-541

1999

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GENETIC FACTORS IN EXTERNAL APICAL ROOT RESORPTION AND ORTHODONTIC TREATMENT

Critical reviews in oral biology and medicine, 2004, Vol.15 (2), p.115-122

2004

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Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation : mapping of the X chromosome breakpoint

American journal of human genetics, 1991-10, Vol.49 (4), p.804-810

1991

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Partners with reciprocal translocations: genetic counseling for the 'double translocation'

Clinical genetics, 1998-05, Vol.53 (5), p.403-407

1998

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Dentin dysplasia, type II linkage to chromosome 4q

Journal of craniofacial genetics and developmental biology, 1997-10, Vol.17 (4), p.172

1997

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The Ephx1(d) allele encoding an Arg338Cys substitution is associated with heat lability

Mammalian genome, 2000-10, Vol.11 (10), p.915-918

2000

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Premature exfoliation of teeth in childhood and adolescence

Advances in pediatrics, 1994, Vol.41 (1), p.453-470

Hartsfield, Jr, J K

1994

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Failure of transcutaneous electrical nerve stimulation in the conventional and burst modes to alter digital skin temperature

Archives of physical medicine and rehabilitation, 1993-02, Vol.74 (2), p.182-187

1993

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Fragile X syndrome: Discordant levels of CGG repeat mosaicism in two brothers

American journal of medical genetics, 1995-08, Vol.60 (4), p.302-306

1995

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Multidisciplinary management of congenital and acquired compensated malocclusions: diagnosis, etiology and treatment planning

Journal of the Indiana Dental Association, 1997, Vol.76 (2), p.42

1997

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Genetic predisposition to external apical root resorption

American journal of orthodontics and dentofacial orthopedics, 2003-03, Vol.123 (3), p.242-252

2003

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Analysis of the EPHX1 113 polymorphism and GSTM1 homozygous null polymorphism and oral clefting associated with maternal smoking

American journal of medical genetics, 2001-07, Vol.102 (1), p.21-24

2001

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Pleiotropy in Coffin-Lowry syndrome: Sensorineural hearing deficit and premature tooth loss as early manifestations

American journal of medical genetics, 1993-03, Vol.45 (5), p.552-557

1993

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Gingival fibromatosis with sensorineural hearing loss: An autosomal dominant trait

American journal of medical genetics, 1985-11, Vol.22 (3), p.623-627

1985

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Cellular and Molecular Pathways Leading to External Root Resorption

The Use of Small Titanium Screws for Orthodontic Anchorage

Genetic and treatment-related risk factors associated with external apical root resorption (EARR) concurrent with orthodontia

Accuracy of mandibular proximal segment position using virtual surgical planning and custom osteosynthesis plates

Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia)

Pathways in external apical root resorption associated with orthodontia

In vitro evaluation of osteoblast responses to carbon nanotube-coated titanium surfaces

Exclusion of Class III Malocclusion Candidate Loci in Brazilian Families

Comparison of reliability in anatomical landmark identification using two-dimensional digital cephalometrics and three-dimensional cone beam computed tomography in vivo

Genetic Predisposition to External Apical Root Resorption in Orthodontic Patients: Linkage of Chromosome-18 Marker

De novo 10q22 interstitial deletion

A novel FGFR2 gene mutation in Crouzon syndrome associated with apparent nonpenetrance

GENETIC FACTORS IN EXTERNAL APICAL ROOT RESORPTION AND ORTHODONTIC TREATMENT

Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation : mapping of the X chromosome breakpoint

Partners with reciprocal translocations: genetic counseling for the 'double translocation'

Dentin dysplasia, type II linkage to chromosome 4q

The Ephx1(d) allele encoding an Arg338Cys substitution is associated with heat lability

Premature exfoliation of teeth in childhood and adolescence

Failure of transcutaneous electrical nerve stimulation in the conventional and burst modes to alter digital skin temperature

Fragile X syndrome: Discordant levels of CGG repeat mosaicism in two brothers

Multidisciplinary management of congenital and acquired compensated malocclusions: diagnosis, etiology and treatment planning

Genetic predisposition to external apical root resorption

Analysis of the EPHX1 113 polymorphism and GSTM1 homozygous null polymorphism and oral clefting associated with maternal smoking

Pleiotropy in Coffin-Lowry syndrome: Sensorineural hearing deficit and premature tooth loss as early manifestations

Gingival fibromatosis with sensorineural hearing loss: An autosomal dominant trait

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