J. Heinrich

发表

Cutting Edge: Decreased Accumulation and Regulatory Function of CD4+CD25high T Cells in Human STAT5b Deficiency1

K. Nadeau, D. Lewis, A. Krensky, 2006, The Journal of Immunology.

Nocturnal TSH Surge and TRH Test Response in the Evaluation of Thyroid Axis in Hypothalamic Pituitary Disorders in Childhood

J. Heinrich, L. Gruñeiro-Papendieck, A. Chiesa, 1998, Hormone Research in Paediatrics.

Deficiency of the circulating insulin-like growth factor system associated with inactivation of the acid-labile subunit gene.

J. Heinrich, Alicia S. Martínez, H. Domené, 2004, The New England journal of medicine.

New observations on midline defects: Coincidence of anophthalmos, microphthalmos and cryptophthalmos with hypothalamic disorders

J. Heinrich, A. Martínez, J. Bierich, 1991, European Journal of Pediatrics.

[Phenotype variability in Noonan syndrome patients with and without PTPN11 mutation].

L. Montenegro, B. Mendonca, I. Arnhold, 2007, Arquivos brasileiros de endocrinologia e metabologia.

Comparison of single and combined tests for the evaluation of plasma growth hormone secretion in normal short children

J. Heinrich, H. Domené, M. Barontini, 1984, Journal of endocrinological investigation.

Pubertal development in male hypopituitarism

M. Rivarola, J. Heinrich, C. Bergadá, 1986, European Journal of Pediatrics.

Antibodies against animal growth hormones appearing in patients treated with human growth hormone: their specificities and influence on growth velocity.

J. Heinrich, H. Domené, C. Peña, 1985, Acta endocrinologica.

Normal Growth Spurt and Final Height despite Low Levels of All Forms of Circulating Insulin-Like Growth Factor-I in a Patient with Acid-Labile Subunit Deficiency

J. Frystyk, Jian-Wen Chen, J. Heinrich, 2007, Hormone Research in Paediatrics.

Estrogen priming effect on growth hormone (GH) provocative test: a useful tool for the diagnosis of GH deficiency.

J. Heinrich, H. Domené, M. Ropelato, 2000, The Journal of clinical endocrinology and metabolism.

17α-Hydroxyprogesterone and Cortisol Serum Levels in Neonates and Young Children: Influence of Age, Gestational Age, Gender and Methodological Procedures

J. Heinrich, A. Chiesa, M. Ropelato, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Growth of Argentinian girls with Turner syndrome.

J. Heinrich, C. Bergadá, A. Martínez, 1995, Annals of human biology.

Heterologous humoral immune response in patients treated with human growth hormone from different sources.

A. Llera, J. Heinrich, H. Domené, 1993, Acta endocrinologica.

Differential Impact of Simple Childhood Obesity on the Components of the Growth Hormone-Insulin-like Growth Factor (IGF)-IGF Binding Proteins Axis

J. Heinrich, H. Domené, M. Ropelato, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

Familial idiopathic hyperphosphatasia (FIH): response to long-term treatment with pamidronate (APD).

J. Heinrich, C. Bergadá, C. Mautalen, 1992, Bone and mineral.

SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.

G. Binder, M. Ranke, V. Hesse, 2004, The Journal of clinical endocrinology and metabolism.

Detection of autoantibodies against hGH in sera of idiopathic hypopituitary children.

A. Llera, J. Heinrich, A. Martínez, 1993, Clinical immunology and immunopathology.

Long‐term endocrine sequelae after surgery, radiotherapy, and chemotherapy in children with medulloblastoma

M. Rivarola, J. Heinrich, Alicia S. Martínez, 1987, Cancer.

The Codon 213 of the 11β-Hydroxysteroid Dehydrogenase Type 2 Gene Is a Hot Spot for Mutations in Apparent Mineralocorticoid Excess1

I. Bergadá, J. Heinrich, D. Rogoff, 1998 .

Phenotypic heterogeneity in familial isolated growth hormone deficiency type I-A.

M. Rivarola, C. Migeon, J. Phillips, 1984, The Journal of clinical endocrinology and metabolism.

Identification of the first patient with a confirmed mutation of the JAK-STAT system

B. Little, L. Bezrodnik, V. Hwa, 2005, Pediatric Nephrology.

Quality of Life in Adults with Growth Hormone Deficiency Diagnosed During Childhood

J. Heinrich, Alicia S. Martínez, C. Bergadá, 2000 .

Trisomy of the Short Stature Homeobox-Containing Gene (SHOX) due to Duplication/Deletion of the X Chomosome: Clinical Implications on the Stature

J. Heinrich, S. Bengolea, H. Jasper, 2010, Hormone Research in Paediatrics.

High serum sex hormone-binding globulin (SHBG) and low serum non-SHBG-bound testosterone in boys with idiopathic hypopituitarism: effect of recombinant human growth hormone treatment.

A. Belgorosky, M. Rivarola, J. Heinrich, 1987, The Journal of clinical endocrinology and metabolism.

Abnormal Responses to TRH in Children Born Small for Gestational Age That Failed to Catch Up

J. Heinrich, A. Chiesa, S. Malozowski, 2009, Hormone Research in Paediatrics.

Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.

P. Donohoue, M. Fassnacht, L. Dunkel, 2005, The Journal of clinical endocrinology and metabolism.

Interstitial deletion of the long arm of chromosome 4, del(4)(q28→q31.3)

S. Copelli, J. Heinrich, R. Coco, 1995 .

Heterozygous IGFALS Gene Variants in Idiopathic Short Stature and Normal Children: Impact on Height and the IGF System

R. Rey, J. Heinrich, Alicia S. Martínez, 2013, Hormone Research in Paediatrics.

Thyroid Dysfunction and High Thyroid Stimulating Hormone Levels in Children with Down's Syndrome

J. Heinrich, A. Chiesa, G. Finkielstain, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Pediatric Graves' Disease: Outcome and Treatment

J. Heinrich, A. Chiesa, G. Finkielstain, 2003 .

Human, bovine, and equine growth hormone antibodies in patients treated with human growth hormone.

J. Heinrich, N. Vita, C. Peña, 1982, The Journal of clinical endocrinology and metabolism.

Growth hormone insensitivity associated with a STAT5b mutation.

B. Little, L. Bezrodnik, V. Hwa, 2003, The New England journal of medicine.

Patterns of TSH response to TRH in children with hypopituitarism.

M. Rivarola, J. Heinrich, C. Bergadá, 1982, The Journal of pediatrics.

Reproducibility and Comparison of Growth Hormone Secretion Tests

J. Heinrich, C. Bergadá, M. Ropelato, 1996, Journal of pediatric endocrinology & metabolism : JPEM.

Growth Follow-up in 100 Children with Congenital Hypothyroidism Before and During Treatment

J. Heinrich, A. Chiesa, C. Bergadá, 1994, The Journal of pediatric endocrinology.

Etiology and association of growth hormone deficiency.

J. Heinrich, C. Bergadá, A. Martínez, 1986, Acta endocrinologica. Supplementum.

Bone age at discontinuation of medroxyprogesterone acetate therapy in girls with precocious puberty: effect on final height.

J. Heinrich, C. Bergadá, A. Martínez, 1995, Hormone Research.

Intermittent hyperaldosteronism in a child due to an adrenal adenoma

I. Bergadá, J. Heinrich, D. Rogoff, 2001, European Journal of Pediatrics.

The codon 213 of the 11beta-hydroxysteroid dehydrogenase type 2 gene is a hot spot for mutations in apparent mineralocorticoid excess.

I. Bergadá, J. Heinrich, D. Rogoff, 1998, Journal of Clinical Endocrinology and Metabolism.

A novel missense mutation in the SH2 domain of the STAT5B gene results in a transcriptionally inactive STAT5b associated with severe IGF-I deficiency, immune dysfunction, and lack of pulmonary disease.

L. Bezrodnik, V. Hwa, P. Fang, 2012, The Journal of clinical endocrinology and metabolism.

Final Height in Long-term Primary Hypothyroid Children

J. Heinrich, A. Chiesa, C. Bergadá, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Treatment of Hypopituitary Children with Synthetic Met-Growth Hormone (Somatrem): Two Years Experience

J. Heinrich, Alicia S. Martínez, C. Bergadá, 1991 .

Contents Vol. 80, 2013

P. Czernichow, G. Rappold, H. Wallaschofski, 2014, Hormone Research in Paediatrics.

Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and Argentina.

P. Mullis, J. Heinrich, L. Gruñeiro-Papendieck, 2003, Thyroid : official journal of the American Thyroid Association.

The C105fs114X Is the Prevalent Thyrotropin Beta-Subunit Gene Mutation in Argentinean Patients with Congenital Central Hypothyroidism

J. Heinrich, L. Gruñeiro-Papendieck, A. Chiesa, 2004, Hormone Research in Paediatrics.

Emergencia pediátrica: insuficiencia suprarrenal aguda Pediatric emergency: adrenal insufficiency and adrenal crisis

J. Heinrich, Alicia S. Martínez, 2010 .

Testicular function in hypopituitarism.

M. Rivarola, E. Podesta, J. Heinrich, 1972, Pediatric research.

EFFECTS OF PROLONGED IGF-I TREATMENT IN CHILDREN WITH GROWTH HORMONE INSENSITIVITY SYNDROME (GHIS)

L. Ghizzoni, P. Backeljauw, D. Donaldson, 1993, Pediatric Research.

Lack of correlation of serum estradiol with growth velocity during male pubertal growth.

A. Belgorosky, M. Rivarola, J. Heinrich, 1989, Acta endocrinologica.