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Mutation in the α-synuclein gene identified in families with Parkinson's disease

Science (American Association for the Advancement of Science), 1997-06, Vol.276 (5321), p.2045-2047

1997

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Divergent Consequences of Success and Failure in Japan and North America: An Investigation of Self-Improving Motivations and Malleable Selves

Journal of personality and social psychology, 2001-10, Vol.81 (4), p.599-615

2001

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Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

Nature genetics, 2000-03, Vol.24 (3), p.283-286

2000

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The role of BRAF(V600E) mutation as poor prognostic factor for the outcome of patients with intrathyroid papillary thyroid carcinoma

Biomedicine & pharmacotherapy, 2014-05, Vol.68 (4), p.413-417

2014

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Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

Science (American Association for the Advancement of Science), 1996-11, Vol.274 (5290), p.1197-1199

1996

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Response to Paclitaxel, Topotecan, and Topotecan-Cyclophosphamide in Children With Untreated Disseminated Neuroblastoma Treated in an Upfront Phase II Investigational Window: A Pediatric Oncology Group Study

Journal of clinical oncology, 2004-10, Vol.22 (20), p.4119-4126

2004

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Eosinophilic esophagitis and double-balloon enteroscopy: a dangerous combination

Endoscopy, 2009, Vol.41 Suppl 2 (S 02), p.E85-E85

2009

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Natural history and biology of stage A neuroblastoma: a Pediatric Oncology Group Study

Journal of pediatric hematology/oncology, 2000-05, Vol.22 (3), p.197-205

2000

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Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease

Neurology, 1996-01, Vol.46 (1), p.208-213

1996

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The gene for pycnodysostosis maps to human chromosome 1cen-q21

Nature genetics, 1995-06, Vol.10 (2), p.238-239

1995

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Evidence for a new spinocerebellar ataxia locus

Movement disorders, 1997-05, Vol.12 (3), p.412-417

1997

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The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease

Arquivos de neuro-psiquiatria, 2001-09, Vol.59 (3-B), p.722-724

2001

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Prognostic significance of age, MYCN oncogene amplification, tumor cell ploidy, and histology in 110 infants with stage D(S) neuroblastoma: the pediatric oncology group experience--a pediatric oncology group study

Journal of clinical oncology, 1998-06, Vol.16 (6), p.2007-2017

1998

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Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiency

Clinical biochemistry, 1997-02, Vol.30 (1), p.79-81

1997

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Genetic staging of unresectable or metastatic neuroblastoma in infants : a pediatric oncology group study

JNCI : Journal of the National Cancer Institute, 1997-03, Vol.89 (5), p.373-380

1997

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The prognostic significance of autologous bone marrow transplant in advanced neuroblastoma

Journal of clinical oncology, 1991-06, Vol.9 (6), p.1045-1049

1991

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The efficacy of thal fundoplication in the treatment of gastroesophageal reflux: The influence of central nervous system impairment

Journal of pediatric surgery, 1988-07, Vol.23 (7), p.638-640

1988

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Bioethics in pediatric neuromuscular disease

Seminars in pediatric neurology, 1998-06, Vol.5 (2), p.124-131

Smith, E. Ide

1998

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Intra-abdominal abscess and peritonitis

Clinical nuclear medicine, 1989-04, Vol.14 (4), p.296-297

1989

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The acute abdomen in the preschool child

Southern medical journal (Birmingham, Ala.), 1966-11, Vol.59 (11), p.1260-1267

1966

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Papillary thyroid microcarcinoma. Long-term outcome in 587 cases compared with published data

Minerva chirurgica, 2007-10, Vol.62 (5), p.315

2007

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Pancreas divisum, pancreatic pseudocyst, and choledochal cyst in an 8-year-old child

Journal of pediatric surgery, 1989, Vol.24 (1), p.52-53

1989

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Brachydactyly type C gene maps to human chromsome 12q24

Genomics (San Diego, Calif.), 1996-11, Vol.38 (1), p.45-50

1996

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Familial congenital diaphragmatic hernia is an autosomal recessive variant

Journal of pediatric surgery, 1989-09, Vol.24 (9), p.860-864

1989

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Imperforate anus: The neurologic implication of sacral abnormalities

Journal of pediatric surgery, 1984-12, Vol.19 (6), p.838-842

1984

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Mutation in the α-synuclein gene identified in families with Parkinson's disease

Divergent Consequences of Success and Failure in Japan and North America: An Investigation of Self-Improving Motivations and Malleable Selves

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

The role of BRAF(V600E) mutation as poor prognostic factor for the outcome of patients with intrathyroid papillary thyroid carcinoma

Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

Response to Paclitaxel, Topotecan, and Topotecan-Cyclophosphamide in Children With Untreated Disseminated Neuroblastoma Treated in an Upfront Phase II Investigational Window: A Pediatric Oncology Group Study

Eosinophilic esophagitis and double-balloon enteroscopy: a dangerous combination

Natural history and biology of stage A neuroblastoma: a Pediatric Oncology Group Study

Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease

The gene for pycnodysostosis maps to human chromosome 1cen-q21

Evidence for a new spinocerebellar ataxia locus

The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease

Prognostic significance of age, MYCN oncogene amplification, tumor cell ploidy, and histology in 110 infants with stage D(S) neuroblastoma: the pediatric oncology group experience--a pediatric oncology group study

Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiency

Genetic staging of unresectable or metastatic neuroblastoma in infants : a pediatric oncology group study

The prognostic significance of autologous bone marrow transplant in advanced neuroblastoma

The efficacy of thal fundoplication in the treatment of gastroesophageal reflux: The influence of central nervous system impairment

Bioethics in pediatric neuromuscular disease

Intra-abdominal abscess and peritonitis

The acute abdomen in the preschool child

Papillary thyroid microcarcinoma. Long-term outcome in 587 cases compared with published data

Pancreas divisum, pancreatic pseudocyst, and choledochal cyst in an 8-year-old child

Brachydactyly type C gene maps to human chromsome 12q24

Familial congenital diaphragmatic hernia is an autosomal recessive variant

Imperforate anus: The neurologic implication of sacral abnormalities

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