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Topical Tacrolimus 0.1% for treatment of cutaneous microcystic lymphatic malformations

Lymphology, 2021, Vol.54 (2), p.106

2021

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A salvage surgical solution for recurrent lymphangioma of the prepuce

British journal of plastic surgery, 2005, Vol.58 (1), p.97-99

2005

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Lymphatic dysplasia in paediatrics. A new classification

International angiology, 1999-03, Vol.18 (1), p.6

Papendieck, C M

1999

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Lipoblastoma-lipoblastomatosis associated with unilateral limb hypertrophy: A case report in a newborn

Lymphology, 2003-06, Vol.36 (2), p.69-73

2003

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Hair Tourniquet syndrome : An unusual cause of perinatologic secondary lymphedema

Lymphology, 1999-12, Vol.32 (4), p.171-172

PAPENDIECK, C. M

1999

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Klippel-Trenaunay-Servelle syndrome in pediatrics

Lymphatic research and biology, 2003, Vol.1 (1), p.81-85

2003

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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

Clinical chemistry (Baltimore, Md.), 2006-02, Vol.52 (2), p.182-191

2006

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Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis

Endocrine, 2022-06, Vol.77 (1), p.86-101

2022

Volltextzugriff (PDF)

Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

Clinical endocrinology (Oxford), 2012-04, Vol.76 (4), p.568-576

2012

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Imaging of lymphatic dysplasia in Noonan syndrome: Case studies and historical atlas

Lymphology, 2021, Vol.54 (1), p.23

2021

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Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7

Clinical endocrinology (Oxford), 2010-01, Vol.72 (1), p.112-121

2010

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Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases

Archivos argentinos de pediatría, 2017-06, Vol.115 (3), p.e162-e165

2017

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Neuroradiological reporting from abroad — /INS;Is it possible?

Journal of the neurological sciences, 2013-10, Vol.333, p.e189-e189

2013

Volltextzugriff (PDF)

Hipotiroidismo congénito transitorio por defectos bialélicos del genDUOX2. Dos casos clínicos

Archivos argentinos de pediatría, 2017-06, Vol.115 (3), p.e162-e165

2017

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Supporting program comprehension in large preprocessor-based software product lines

IET software, 2012-12, Vol.6 (6), p.488-488

2012

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Genotyping of resistance to thyroid hormone in South American population. Identification of seven novel missense mutations in the human thyroid hormone receptor β gene

Molecular and cellular probes, 2009-06, Vol.23 (3-4), p.148-153

2009

Volltextzugriff (PDF)

Production and Characterization of Saratin, an Inhibitor of von Willebrand Factor-Dependent Platelet Adhesion to Collagen

Seminars in thrombosis and hemostasis, 2001-08, Vol.27 (4), p.337-348

2001

Volltextzugriff (PDF)

The C105fs114X is the prevalent thyrotropin beta-subunit gene mutation in Argentinean patients with congenital central hypothyroidism

Hormone research, 2004-01, Vol.61 (1), p.41-46

2004

Volltextzugriff (PDF)

Lymphedema: Complete Medical and Surgical Management

1, 2015

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Using background colors to support program comprehension in software product lines

15th Annual Conference on Evaluation & Assessment in Software Engineering (EASE 2011), 2011, p.66-75

2011

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High incidence of thyroid disturbances in 49 children with Turner syndrome

The Journal of pediatrics, 1987-08, Vol.111 (2), p.258-261

1987

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Basal TSH vs TRH/TSH Test with Sensitive Methods in Pediatrics

Pediatric research, 1999-03, Vol.45 (3), p.438-438

1999

Volltextzugriff (PDF)

VARIATIONS IN CLINICAL, HORMONAL AND SEROLOGICAL EXPRESSIONS OF CHRONIC LYMPHOCYTIC THYROIDITIS (CLT) IN CHILDREN AND ADOLESCENTS

Clinical endocrinology (Oxford), 1982-01, Vol.16 (1), p.19-28

1982

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23. JUVENILE HYPERTHYROIDISM (J H): THERAPEUTIC OPTIONS ACCORDING TO THE PREDICTION OF THE EVOLUTION

Pediatric research, 1988-06, Vol.23 (6), p.651-651

1988

Volltextzugriff (PDF)

Patterns of TSH response to TRH in children with hypopituitarism

The Journal of pediatrics, 1982-03, Vol.100 (3), p.387-392

1982

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Topical Tacrolimus 0.1% for treatment of cutaneous microcystic lymphatic malformations

A salvage surgical solution for recurrent lymphangioma of the prepuce

Lymphatic dysplasia in paediatrics. A new classification

Lipoblastoma-lipoblastomatosis associated with unilateral limb hypertrophy: A case report in a newborn

Hair Tourniquet syndrome : An unusual cause of perinatologic secondary lymphedema

Klippel-Trenaunay-Servelle syndrome in pediatrics

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

Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis

Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

Imaging of lymphatic dysplasia in Noonan syndrome: Case studies and historical atlas

Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7

Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases

Neuroradiological reporting from abroad — /INS;Is it possible?

Hipotiroidismo congénito transitorio por defectos bialélicos del genDUOX2. Dos casos clínicos

Supporting program comprehension in large preprocessor-based software product lines

Genotyping of resistance to thyroid hormone in South American population. Identification of seven novel missense mutations in the human thyroid hormone receptor β gene

Production and Characterization of Saratin, an Inhibitor of von Willebrand Factor-Dependent Platelet Adhesion to Collagen

The C105fs114X is the prevalent thyrotropin beta-subunit gene mutation in Argentinean patients with congenital central hypothyroidism

Lymphedema: Complete Medical and Surgical Management

Using background colors to support program comprehension in software product lines

High incidence of thyroid disturbances in 49 children with Turner syndrome

Basal TSH vs TRH/TSH Test with Sensitive Methods in Pediatrics

VARIATIONS IN CLINICAL, HORMONAL AND SEROLOGICAL EXPRESSIONS OF CHRONIC LYMPHOCYTIC THYROIDITIS (CLT) IN CHILDREN AND ADOLESCENTS

23. JUVENILE HYPERTHYROIDISM (J H): THERAPEUTIC OPTIONS ACCORDING TO THE PREDICTION OF THE EVOLUTION

Patterns of TSH response to TRH in children with hypopituitarism

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