R. Lala

发表

Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society

P. Bianco, F. Grill, E. Ippolito, 2003, Journal of pediatric orthopedics. Part B.

R. Lala, G. Monti, F. Savino, 2008, Annals of Nutrition and Metabolism.

Teriparatide (rhPTH) treatment in children with syndromic hypoparathyroidism

A. Mussa, R. Lala, P. Matarazzo, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

Early hormonal and surgical treatment of cryptorchidism.

R. Lala, C. de Sanctis, P. Matarazzo, 1997, The Journal of urology.

McCune-Albright Syndrome: Persistence of Autonomous Ovarian Hyperfunction During Adolescence and Early Adult Age

V. De Sanctis, R. Lala, F. Rigon, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Altered Bone Mineral Density in Patients with Complete Androgen Insensitivity Syndrome

G. Saggese, M. Cappa, R. Lala, 1998, Hormone Research in Paediatrics.

HLA Haplotypes and Hormonal Studies in 25 Italian Families of Patients with Classical and Non-classical 21-OH Deficiency

R. Lala, E. Curtoni, C. de Sanctis, 1994, The Journal of pediatric endocrinology.

Cushing syndrome due to ectopic adrenocorticotropic hormone secretion in a 3-year-old child

M. Papotti, I. Rabbone, R. Lala, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

A new test for the diagnosis of growth hormone deficiency due to primary pituitary impairment: combined administration of pyridostigmine and growth hormone-releasing hormone

E. Arvat, E. Ghigo, M. Boghen, 1990, Journal of endocrinological investigation.

Pamidronate treatment of bone fibrous dysplasia in nine children with McCune‐Albright syndrome

R. Lala, F. Rigon, S. Bertelloni, 2000, Acta paediatrica.

HDR syndrome: A novel “de novo” mutation in GATA3 gene

R. Lala, A. Ponzone, E. Garelli, 2009, American journal of medical genetics. Part A.

Bone Metabolism in Thalassemia a

A. Piga, R. Lala, G. Isaia, 1998, Annals of the New York Academy of Sciences.

Bone density and metabolism in thalassaemia.

A. Piga, R. Lala, G. Isaia, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

R. Lala, S. Pagliardini, A. Corrias, 1993, The Journal of pediatric endocrinology.

Phalangeal quantitative ultrasound in children with phenylketonuria: a pilot study.

A. Mussa, R. Lala, F. Porta, 2008, Ultrasound in medicine & biology.

Testicular microlithiasis: an unreported feature of McCune-Albright syndrome in males.

R. Lala, S. Bertelloni, G. Weber, 2004, The Journal of pediatrics.

Heart‐hand syndrome II. A report of Tabatznik syndrome with new findings

M. Silengo, R. Lala, A. Guala, 1990, Clinical genetics.

ARGININE POTENTIATES THE GHRH‐ BUT NOT THE PYRIDOSTIGMINE‐INDUCED GH SECRETION IN NORMAL SHORT CHILDREN. FURTHER EVIDENCE FOR A SOMATOSTATIN SUPPRESSING EFFECT OF ARGININE

E. Ghigo, R. Lala, F. Camanni, 1990, Clinical endocrinology.

Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disorders

F. Terlizzi, A. Mussa, R. Lala, 2012, Osteoporosis International.

Sex attribution, gender identity and quality of life in disorders of sex development due to 45,X/46,XY mosaicism: methods for clinical and psychosocial assessment

Angela M Caldarera, C. Crespi, R. Lala, 2015, AIMS Genetics.

Bone mass and metabolism in thalassemic children and adolescents treated with different iron-chelating drugs

A. Piga, R. Lala, G. Isaia, 2003, Journal of Bone and Mineral Metabolism.

Growth hormone—Insulin‐like growth factor 1 axis hyperactivity on bone fibrous dysplasia in McCune‐Albright Syndrome

M. Collins, M. Zacharin, R. Lala, 2018, Clinical endocrinology.

Laparoscopic Management of Ovarian Cystsin Peripheral Precocious Puberty of McCune-Albright Syndrome

R. Lala, L. De Sanctis, P. Matarazzo, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

An R201H activating mutation of the GNAS1 (Gsα) gene in a corticotroph pituitary adenoma

M. Collins, P. Bianco, A. Corsi, 2002, Molecular pathology : MP.

A Novel GNAS1 Mutation, R201G, in McCune–Albright Syndrome

P. Bianco, A. Majolagbe, A. Corsi, 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients

M. Segni, M. Cisternino, L. Ghizzoni, 1999, Journal of pediatric endocrinology & metabolism : JPEM.

Intersexual Births: The Epistemology of Sex and Ethics of Sex Assignment

R. Lala, Elena Nave, M. Cresti, 2018, Journal of Bioethical Inquiry.

Emotional Burden and Coping Strategies of Parents of Children with Rare Diseases

L. Ostacoli, R. Picci, F. Oliva, 2013, Journal of Child and Family Studies.

Image Diagnosis in McCune-Albright Syndrome

A. Mussa, R. Lala, C. Defilippi, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Thyroid Abnormalities in Children and Adolescents with McCune-Albright Syndrome

R. Lala, M. Vigone, M. Wasniewska, 2012, Hormone Research in Paediatrics.

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

J. Seidman, B. Bruneau, M. Bamshad, 1997, Nature Genetics.

Isolated adrenocorticotropic hormone deficiency associated with common variable immunodeficiency

R. Lala, P. Tovo, C. Sanctis, 1991, European Journal of Pediatrics.

Testicular function in men treated in childhood for undescended testes.

R. Lala, F. Canavese, S. Vinardi, 2001, Journal of pediatric surgery.

Improved Sperm Count and Motility in Young Men Surgically Treated for Cryptorchidism in the First Year of Life

A. Mussa, R. Lala, F. Feyles, 2013, European Journal of Pediatric Surgery.

Combined therapy with LHRH and HCG in cryptorchid infants

R. Lala, F. Hadžiselimović, C. Sanctis, 2005, European Journal of Pediatrics.

Early medical and surgical treatment of cryptorchidism: clinical, anatomic, and histologic findings

R. Lala, F. Hadžiselimović, C. Sanctis, 1992, Pediatric Surgery International.

Primary immature mediastinal teratoma in a newborn.

R. Lala, B. Das, S. Sahoo, 2001, Indian pediatrics.

Cryptorchidism: medical and surgical treatment in the 1st year of life

R. Lala, C. de Sanctis, F. Canavese, 1998, Pediatric Surgery International.

Non-Palpable Testes. Orchiopexy in Single Stage

R. Lala, C. de Sanctis, C. Sanctis, 1995, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Homeobox HOXA10 Gene Analysis in Cryptorchidism

P. Simi, C. Foresta, R. Lala, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

Sperm Count of Young Men Surgically Treated for Cryptorchidism in the First and Second Year of Life: Fertility is Better in Children Treated at a Younger Age

A. Mussa, R. Lala, L. Ferrero, 2009, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Growth impairment, IGF I hyposecretion and thyroid dysfunction in children with perinatal HIV‐1 infection

R. Lala, P. Matarazzo, E. Palomba, 1994, Acta paediatrica.

Mechanism of origin in two cases of chimerism

M. Repici, S. Cristina, R. Lala, 2011 .

Molecular Analysis of the GNAS1 Gene for the Correct Diagnosis of Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism

M. Maghnie, I. Dianzani, S. Maio, 2003, Pediatric Research.

Pubertal development in patients with McCune-Albright syndrome or pseudohypoparathyroidism.

R. Lala, C. de Sanctis, L. De Sanctis, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

Emotional Burden and Coping Strategies of Parents of Children with Rare Diseases

L. Ostacoli, R. Picci, F. Oliva, 2015 .

Low birth-weight, microcephalic malformation syndrome in a 46,XX girl and her 46,XY sister with agonadism: third report of the Kennerknecht syndrome or autosomal recessive Seckel-like syndrome with previously undescribed genital anomalies.

R. Lala, M. Silengo, A. Linari, 2001, American journal of medical genetics.

Effectiveness of primary inguinal orchiopexy as treatment of non-palpable testes in the first two years of age.

R. Lala, L. Valfré, F. Canavese, 2010, Minerva pediatrica.

Bone Turnover in Children and Adolescents with McCune-Albright Syndrome Treated with Pamidronate for Bone Fibrous Dysplasia

G. Priolo, R. Lala, G. Isaia, 2002, Calcified Tissue International.

20 novel point mutations and one large deletion in EXT1 and EXT2 genes: report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis.

M. Ciavarella, B. Pasini, M. Bengala, 2013, Gene.

Endocrine Function and Water Metabolism in Children and Adolescents with Surgically Treated Intra/Parasellar Tumors

R. Lala, L. Genitori, C. de Sanctis, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

Management of sodium metabolism derangements in children treated for hypothalamic-hypophyseal tumors

A. Mussa, R. Lala, P. Matarazzo, 2010, Journal of Pediatric Biochemistry.

Odontoiatric perspectives and osteonecrosis of the jaw as a possible adverse effect of bisphosphonates therapy in fibrous dysplasia and McCune-Albright syndrome

R. Lala, P. Defabianis, P. Matarazzo, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Mutations in human TBX3 alter limb, apocrine, and genital development in ulnar-mammary syndrome

J. Seidman, B. Bruneau, M. Bamshad, 1998, Nature Genetics.

Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

N. Bresolin, G. Comi, C. Doriguzzi, 1989, Journal of neurology, neurosurgery, and psychiatry.

Combined treatment with bicalutamide and anastrozole in a young boy with peripheral precocious puberty due to McCune-Albright Syndrome.

A. Mussa, R. Lala, P. Matarazzo, 2012, Endocrine journal.

Genetics of McCune-Albright Syndrome

R. Lala, C. de Sanctis, L. De Sanctis, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Bisphosphonate Treatment of Bone Fibrous Dysplasia in McCuneAlbright Syndrome

R. Lala, A. Corrias, J. Bellone, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Impact of endocrine hyperfunction and phosphate wasting on bone in McCune-Albright syndrome.

R. Lala, C. Defilippi, C. de Sanctis, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Diagnosis and medical-surgical treatment of cryptorchidism

R. Lala, C. Sanctis, 2000, Journal of endocrinological investigation.

Pamidronate treatment in bone fibrous dysplasia in children and adolescents with McCune-Albright syndrome.

R. Lala, C. de Sanctis, P. Matarazzo, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Sonographic Appearance of Ovaries and Gonadotropin Secretions as Prognostic Tools of Spontaneous Puberty in Girls with Turner's Syndrome

R. Lala, C. de Sanctis, P. Matarazzo, 1995, Journal of pediatric endocrinology & metabolism : JPEM.

Laparoscopic Unilateral Adrenalectomy in Children for Isolated Primary Pigmented Nodular Adrenocortical Disease (PPNAD): Case Report and Literature Review

M. Repici, B. Pasini, R. Lala, 2010, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Changing Pattern of Femoral Deformity During Growth in Polyostotic Fibrous Dysplasia of the Bone: An Analysis of 46 Cases

R. Sorge, P. Farsetti, E. Ippolito, 2016, Journal of pediatric orthopedics.

Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family

I. Dianzani, R. Lala, A. Pucci, 2006, Journal of Clinical Pathology.

Multiple Bone Fractures in an 8-Year-Old Child with Cow’s Milk Allergy and Inappropriate Calcium Supplementation

R. Miniero, R. Lala, F. Savino, 2007, Annals of Nutrition and Metabolism.

Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome.

R. Lala, P. Matarazzo, P. Franceschini, 1992, American journal of medical genetics.

Continuous subcutaneous hydrocortisone infusion (CSHI) in a young adolescent with congenital adrenal hyperplasia (CAH)

F. Cerutti, I. Rabbone, R. Lala, 2011, Journal of pediatric endocrinology & metabolism : JPEM.