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R. Lala · SciRah

Researcher profile · Semantic Scholar

R. Lala

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R. Lala — researcher profile on SciRah

h-index: 27
Works: 89
Citations: 2,628

Most-cited papers

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
M. Bamshad, R. C. Lin, David J. Law, W. Watkins +11 more
1997Nature Genetics523 citations Open access
Semantic Scholar
Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society
E. Ippolito, E. Bray, A. Corsi, F. De Maio +10 more
2003Journal of pediatric orthopedics. Part B193 citations
Semantic Scholar
Pamidronate treatment of bone fibrous dysplasia in nine children with McCune‐Albright syndrome
R. Lala, P. Matarazzo, S. Bertelloni, F. Buzi +2 more
2000Acta paediatrica118 citations
Semantic Scholar
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, J. Bellone, E. Mazza, E. Imperiale +5 more
1990Clinical Endocrinology98 citations
Semantic Scholar
Altered Bone Mineral Density in Patients with Complete Androgen Insensitivity Syndrome
S. Bertelloni, G. Baroncelli, G. Federico, M. Cappa +2 more
1998Hormone Research in Paediatrics97 citations
Semantic Scholar
Mutations in human TBX3 alter limb, apocrine, and genital development in ulnar-mammary syndrome
M. Bamshad, R. C. Lin, David J. Law, W. Watkins +11 more
1998Nature Genetics80 citations Open access
Semantic Scholar
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
F. Canavese, A. Mussa, M. Manenti, M. Cortese +4 more
2009European journal of pediatric surgery71 citations
Semantic Scholar
An R201H activating mutation of the GNAS1 (Gsα) gene in a corticotroph pituitary adenoma
M. Riminucci, M. Collins, R. Lala, A. Corsi +3 more
2002Molecular Pathology67 citations Open access
Semantic Scholar
Emotional Burden and Coping Strategies of Parents of Children with Rare Diseases
R. Picci, F. Oliva, Federica Trivelli, C. Carezana +4 more
2013Journal of Child and Family Studies65 citations Open access
Semantic Scholar
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family
M. Campagnoli, A. Pucci, E. Garelli, A. Carando +6 more
2006Journal of Clinical Pathology63 citations Open access
Semantic Scholar
A Novel GNAS1 Mutation, R201G, in McCune–Albright Syndrome
M. Riminucci, Larry W. Fisher, Adesola Majolagbe, A. Corsi +4 more
1999Journal of Bone and Mineral Research61 citations Open access
Semantic Scholar
Thyroid Abnormalities in Children and Adolescents with McCune-Albright Syndrome
D. Tessaris, A. Corrias, P. Matarazzo, L. de Sanctis +4 more
2012Hormone Research in Paediatrics57 citations
Semantic Scholar
Bone mass and metabolism in thalassemic children and adolescents treated with different iron-chelating drugs
M. D. Di Stefano, P. Chiabotto, C. Roggia, F. Garofalo +3 more
2003Journal of Bone and Mineral Metabolism56 citations
Semantic Scholar
Molecular Analysis of the GNAS1 Gene for the Correct Diagnosis of Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism
L. de Sanctis, D. Romagnolo, M. Olivero, F. Buzi +12 more
2003Pediatric Research55 citations
Semantic Scholar
Testicular function in men treated in childhood for undescended testes.
S. Vinardi, P. Magro, M. Manenti, R. Lala +3 more
2001Journal of Pediatric Surgery53 citations
Semantic Scholar
Bone Turnover in Children and Adolescents with McCune-Albright Syndrome Treated with Pamidronate for Bone Fibrous Dysplasia
G. Isaia, R. Lala, C. Defilippi, P. Matarazzo +4 more
2002Calcified Tissue International52 citations
Semantic Scholar
HDR syndrome: A novel “de novo” mutation in GATA3 gene
S. Ferraris, Angelo Del Monaco, E. Garelli, A. Carando +4 more
2009American Journal of Medical Genetics. Part A48 citations
Semantic Scholar
Bisphosphonate Treatment of Bone Fibrous Dysplasia in McCuneAlbright Syndrome
R. Lala, P. Matarazzo, M. Andreo, D. Marzari +4 more
2006Journal of Pediatric Endocrinology & Metabolism (JPEM)47 citations
Semantic Scholar
Improved Sperm Count and Motility in Young Men Surgically Treated for Cryptorchidism in the First Year of Life
Francesca Feyles, Valentina Peiretti, A. Mussa, M. Manenti +3 more
2013European journal of pediatric surgery46 citations
Semantic Scholar
Pamidronate treatment in bone fibrous dysplasia in children and adolescents with McCune-Albright syndrome.
P. Matarazzo, R. Lala, G. Masi, M. Andreo +2 more
2002Journal of Pediatric Endocrinology & Metabolism (JPEM)42 citations
Semantic Scholar
Homeobox HOXA10 Gene Analysis in Cryptorchidism
V. Bertini, S. Bertelloni, A. Valetto, R. Lala +2 more
2004Journal of Pediatric Endocrinology & Metabolism (JPEM)37 citations
Semantic Scholar
Testicular microlithiasis: an unreported feature of McCune-Albright syndrome in males.
M. Wasniewska, F. de Luca, S. Bertelloni, P. Matarazzo +4 more
2004Jornal de Pediatria36 citations
Semantic Scholar
Bone Metabolism in Thalassemia a
F. Garofalo, A. Piga, R. Lala, S. Chiabotto +2 more
1998Annals of the New York Academy of Sciences35 citations
Semantic Scholar
Growth impairment, IGF I hyposecretion and thyroid dysfunction in children with perinatal HIV‐1 infection
P. Matarazzo, E. Palomba, R. Lala, E. Ciuti +3 more
1994Acta paediatrica34 citations
Semantic Scholar
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. Ghigo, E. Imperiale, G. Boffano, E. Mazza +11 more
1990Journal of Endocrinological Investigation33 citations
Semantic Scholar
Bone density and metabolism in thalassaemia.
R. Lala, P. Chiabotto, M. D. Di Stefano, G. Isaia +2 more
1998Journal of Pediatric Endocrinology & Metabolism (JPEM)30 citations
Semantic Scholar
Growth hormone—Insulin-like growth factor 1 axis hyperactivity on bone fibrous dysplasia in McCune-Albright Syndrome
D. Tessaris, A. Boyce, M. Zacharin, P. Matarazzo +3 more
2018Clinical Endocrinology28 citations Open access
Semantic Scholar
Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
S. Einaudi, R. Lala, A. Corrias, P. Matarazzo +2 more
1993Journal of Pediatric Endocrinology28 citations
Semantic Scholar
Teriparatide (rhPTH) treatment in children with syndromic hypoparathyroidism
P. Matarazzo, G. Tuli, L. Fiore, A. Mussa +3 more
2019Journal of Pediatric Endocrinology & Metabolism (JPEM)27 citations
Semantic Scholar
Long-term outcome of male-limited gonadotropin-independent precocious puberty.
S. Bertelloni, G. Baroncelli, R. Lala, M. Cappa +3 more
1997Hormone Research27 citations
Semantic Scholar
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, M. Coco, Filomena Baorda, P. Stanziale +15 more
2013Gene25 citations
Semantic Scholar
Cushing syndrome due to ectopic adrenocorticotropic hormone secretion in a 3-year-old child
P. Matarazzo, G. Tuli, D. Tessaris, F. Verna +9 more
2011Journal of Pediatric Endocrinology & Metabolism (JPEM)25 citations
Semantic Scholar
Genetics of McCune-Albright Syndrome
L. de Sanctis, L. Del Mastro, M. C. Russo, P. Matarazzo +2 more
2006Journal of Pediatric Endocrinology & Metabolism (JPEM)25 citations
Semantic Scholar
McCune-Albright Syndrome: Persistence of Autonomous Ovarian Hyperfunction During Adolescence and Early Adult Age
P. Matarazzo, R. Lala, M. Andreo, S. Einaudi +10 more
2006Journal of Pediatric Endocrinology & Metabolism (JPEM)25 citations
Semantic Scholar
Combined treatment with bicalutamide and anastrozole in a young boy with peripheral precocious puberty due to McCune-Albright Syndrome.
D. Tessaris, P. Matarazzo, A. Mussa, G. Tuli +3 more
2012Endocrine journal24 citations Open access
Semantic Scholar
Continuous subcutaneous hydrocortisone infusion (CSHI) in a young adolescent with congenital adrenal hyperplasia (CAH)
G. Tuli, I. Rabbone, S. Einaudi, Valeria di Gianni +4 more
2011Journal of Pediatric Endocrinology & Metabolism (JPEM)23 citations
Semantic Scholar
Heart‐hand syndrome II. A report of Tabatznik syndrome with new findings
M. Silengo, M. Biagioli, Andrea Guala, G. Lopez‐Bell +1 more
1990Clinical Genetics23 citations
Semantic Scholar
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.
C. Doriguzzi, L. Palmucci, T. Mongini, N. Bresolin +3 more
1989Journal of Neurology Neurosurgery & Psychiatry22 citations Open access
Semantic Scholar
Changing Pattern of Femoral Deformity During Growth in Polyostotic Fibrous Dysplasia of the Bone: An Analysis of 46 Cases
E. Ippolito, M. B. Valentini, R. Lala, F. De Maio +2 more
2016Journal of pediatric orthopedics21 citations
Semantic Scholar
Multiple Bone Fractures in an 8-Year-Old Child with Cow’s Milk Allergy and Inappropriate Calcium Supplementation
G. Monti, V. Libanore, L. Marinaro, R. Lala +2 more
2007Annals of Nutrition and Metabolism21 citations
Semantic Scholar
Phalangeal quantitative ultrasound in children with phenylketonuria: a pilot study.
Francesco Porta, M. Spada, R. Lala, A. Mussa
2008Ultrasound in Medicine and Biology20 citations
Semantic Scholar
Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome.
P. Franceschini, M. P. Vardeu, L. Dalforno, F. Signorile +3 more
1992American journal of medical genetics18 citations
Semantic Scholar
Endocrine Function and Water Metabolism in Children and Adolescents with Surgically Treated Intra/Parasellar Tumors
P. Matarazzo, Lorenzo Genitori, R. Lala, M. Andreo +2 more
2004Journal of Pediatric Endocrinology & Metabolism (JPEM)17 citations
Semantic Scholar
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.
M. Silengo, Angelo Del Monaco, Alessandra Linari, R. Lala
2001American journal of medical genetics17 citations
Semantic Scholar
Non-Palpable Testes. Orchiopexy in Single Stage
F. Canavese, M. Cortese, F. Gennari, R. Gesmundo +3 more
1995European journal of pediatric surgery16 citations
Semantic Scholar
Isolated adrenocorticotropic hormone deficiency associated with common variable immunodeficiency
P. Tovo, R. Lala, S. Martino, G. Pastorelli +1 more
1991European Journal of Pediatrics16 citations
Semantic Scholar
Odontoiatric perspectives and osteonecrosis of the jaw as a possible adverse effect of bisphosphonates therapy in fibrous dysplasia and McCune-Albright syndrome
D. Tessaris, P. Matarazzo, R. Lala, P. Defabianis
2016Journal of Pediatric Endocrinology & Metabolism (JPEM)14 citations
Semantic Scholar
Persistent hyperestrogenism after precocious puberty in young females with McCune-Albright syndrome.
R. Lala, M. Andreo, A. Pucci, P. Matarazzo
2007Pediatric Endocrinology Reviews: diabetes, nutrition, metabolism14 citations
Semantic Scholar
Intersexual Births: The Epistemology of Sex and Ethics of Sex Assignment
Matteo Cresti, Elena Nave, R. Lala
2018Journal of Bioethical Inquiry13 citations Open access
Semantic Scholar
Searching for Arg201 mutations in the GNAS1 gene in Italian patients with McCune-Albright syndrome.
L. de Sanctis, D. Romagnolo, N. Greggio, L. Genitori +2 more
2002Journal of Pediatric Endocrinology & Metabolism (JPEM)10 citations
Semantic Scholar

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G. Tuli — researcher profile on SciRah

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