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Dermatology (Basel, Switzerland)
|
October 4, 2007
SACRAL syndrome
Beth Drolet, Maria Garzon
Frontiers in Pediatrics
|
September 1, 2015
Use of Thrombopoietin Receptor Agonists in Childhood Immune Thrombocytopenia
Angelica Maria Garzon, William Beau Mitchell
Pediatric Dermatology
|
August 16, 2019
Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
Margaret Dowd, Nina Antonov, Maria Garzon, et al.
Archives of Pediatrics & Adolescent Medicine
|
June 10, 2010
Picture of the month. Meningocele
Meaghan Daly, Channing Barnett, Neil Feldstein, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
January 29, 2011
A novel mutation causing pseudohypoparathyroidism 1A with congenital hypothyroidism and osteoma cutis
Tamar Lubell, Maria Garzon, Kwame Anyane Yeboa, et al.
Pediatric Dermatology
|
September 9, 2017
Shedding Light on Alopecia Areata in Pediatrics: A Retrospective Analysis of Comorbidities in Children in the National Alopecia Areata Registry
Jennifer Sorrell, Lynn Petukhova, Rachel Reingold, et al.
Dermatology (Basel, Switzerland)
|
June 9, 2005
Netherton syndrome with extensive skin peeling and failure to thrive due to a homozygous frameshift mutation in SPINK5
Adam S Geyer, Paulina Ratajczak, Marlyanne Pol-Rodriguez, et al.
Pediatric Dermatology
|
June 6, 2003
Generalized acanthosis nigricans in an otherwise healthy young child
Hendrik Uyttendaele, Tamara Koss, Bita Bagheri, et al.
The Journal of Pediatrics
|
November 28, 2017
A Novel Mutation in Junctional Plakoglobin Causing Lethal Congenital Epidermolysis Bullosa
Veronica Rotemberg, Maria Garzon, Christine Lauren, et al.
Journal of Neurosurgical Anesthesiology
|
September 6, 2014
Pediatric surgeons and anesthesiologists expand the dialogue on the neurotoxicity question, rationale for early and delayed surgeries, and practice changes while awaiting definitive evidence
Mary W Byrne, Pasquale Casale, Maria Garzon, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Dermatology (Basel, Switzerland)
|
October 4, 2007
SACRAL syndrome
Beth Drolet, Maria Garzon
Frontiers in Pediatrics
|
September 1, 2015
Use of Thrombopoietin Receptor Agonists in Childhood Immune Thrombocytopenia
Angelica Maria Garzon, William Beau Mitchell
Pediatric Dermatology
|
August 16, 2019
Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
Margaret Dowd, Nina Antonov, Maria Garzon, et al.
Archives of Pediatrics & Adolescent Medicine
|
June 10, 2010
Picture of the month. Meningocele
Meaghan Daly, Channing Barnett, Neil Feldstein, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
January 29, 2011
A novel mutation causing pseudohypoparathyroidism 1A with congenital hypothyroidism and osteoma cutis
Tamar Lubell, Maria Garzon, Kwame Anyane Yeboa, et al.
Pediatric Dermatology
|
September 9, 2017
Shedding Light on Alopecia Areata in Pediatrics: A Retrospective Analysis of Comorbidities in Children in the National Alopecia Areata Registry
Jennifer Sorrell, Lynn Petukhova, Rachel Reingold, et al.
Dermatology (Basel, Switzerland)
|
June 9, 2005
Netherton syndrome with extensive skin peeling and failure to thrive due to a homozygous frameshift mutation in SPINK5
Adam S Geyer, Paulina Ratajczak, Marlyanne Pol-Rodriguez, et al.
Pediatric Dermatology
|
June 6, 2003
Generalized acanthosis nigricans in an otherwise healthy young child
Hendrik Uyttendaele, Tamara Koss, Bita Bagheri, et al.
The Journal of Pediatrics
|
November 28, 2017
A Novel Mutation in Junctional Plakoglobin Causing Lethal Congenital Epidermolysis Bullosa
Veronica Rotemberg, Maria Garzon, Christine Lauren, et al.
Journal of Neurosurgical Anesthesiology
|
September 6, 2014
Pediatric surgeons and anesthesiologists expand the dialogue on the neurotoxicity question, rationale for early and delayed surgeries, and practice changes while awaiting definitive evidence
Mary W Byrne, Pasquale Casale, Maria Garzon, et al.
Page
of 3