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1
Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature
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Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature

Homma, Thais K. ; Freire, Bruna L. ; Honjo, Rachel ; Dauber, Andrew ; Funari, Mariana F.A. ; Lerario, Antonio M. ; Albuquerque, Edoarda V.A. ; Vasques, Gabriela A. ; Bertola, Debora R. ; Kim, Chong A. ; Malaquias, Alexsandra C. ; Jorge, Alexander A.L.

Hormone research in paediatrics, 2020-01, Vol.92 (2), p.115-123 [Periódico revisado por pares]

Basel, Switzerland

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2
Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause
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Artigo
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Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause

Homma, Thais K. ; Krepischi, Ana C.V. ; Furuya, Tatiane K. ; Honjo, Rachel S. ; Malaquias, Alexsandra C. ; Bertola, Debora R. ; Costa, Silvia S. ; Canton, Ana P. ; Roela, Rosimeire A. ; Freire, Bruna L. ; Kim, Chong A. ; Rosenberg, Carla ; Jorge, Alexander A.L.

Hormone research in paediatrics, 2018-01, Vol.89 (1), p.13-21 [Periódico revisado por pares]

Basel, Switzerland

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3
Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan Syndrome
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Artigo
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Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan Syndrome

Malaquias, Alexsandra C. ; Noronha, Renata M. ; Souza, Thaiana T.O. ; Homma, Thais K. ; Funari, Mariana F.A. ; Yamamoto, Guilherme L. ; Silva, Fernanda Viana ; Moraes, Michelle B. ; Honjo, Rachel S. ; Kim, Chong A. ; Nesi-França, Suzana ; Carvalho, Julienne A.R. ; Quedas, Elisangela P.S. ; Bertola, Debora R. ; Jorge, Alexander A.L.

Hormone research in paediatrics, 2019-01, Vol.91 (4), p.252-261 [Periódico revisado por pares]

Basel, Switzerland

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4
Clinical Characterization and Analysis of the SRD5A2 Gene in Six Korean Patients with 5α-Reductase Type 2 Deficiency
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Artigo
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Clinical Characterization and Analysis of the SRD5A2 Gene in Six Korean Patients with 5α-Reductase Type 2 Deficiency

Ko, Jung Min ; Cheon, Chong-Kun ; Kim, Gu-Hwan ; Kim, Sung Hoon ; Kim, Kun Suk ; Yoo, Han-Wook

Hormone research in paediatrics, 2010-01, Vol.73 (1), p.41-48 [Periódico revisado por pares]

Basel, Switzerland

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5
Three Novel Pathogenic Mutations in KATP Channel Genes and Somatic Imprinting Alterations of the 11p15 Region in Pancreatic Tissue in Patients with Congenital Hyperinsulinism
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Artigo
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Three Novel Pathogenic Mutations in KATP Channel Genes and Somatic Imprinting Alterations of the 11p15 Region in Pancreatic Tissue in Patients with Congenital Hyperinsulinism

Lee, Beom Hee ; Lee, Jin ; Kim, Jae-Min ; Kang, Minji ; Kim, Gu-Hwan ; Choi, Jin-Ho ; Kim, Jihun ; Kim, Chong Jai ; Kim, Dae-Yeon ; Kim, Seong-Chul ; Yoo, Han-Wook

Hormone research in paediatrics, 2015-04, Vol.83 (3), p.204-210 [Periódico revisado por pares]

Basel, Switzerland: S. Karger AG

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6
Clinical Characterization and Analysis of the SRD5A2 Gene in Six Korean Patients with 5[alpha]-Reductase Type 2 Deficiency
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Artigo
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Clinical Characterization and Analysis of the SRD5A2 Gene in Six Korean Patients with 5[alpha]-Reductase Type 2 Deficiency

Ko, Jung Min ; Cheon, Chong-kun ; Kim, Gu-hwan ; Kim, Sung Hoon ; Kim, Kun Suk ; Yoo, Han-wook

Hormone research in paediatrics, 2010-01, Vol.73 (1), p.41 [Periódico revisado por pares]

Basel: S. Karger AG

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7
Clinical characterization and analysis of the SRD5A2 gene in six Korean patients with 5alpha-reductase type 2 deficiency
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Artigo
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Clinical characterization and analysis of the SRD5A2 gene in six Korean patients with 5alpha-reductase type 2 deficiency

Ko, Jung Min ; Cheon, Chong-Kun ; Kim, Gu-Hwan ; Kim, Sung Hoon ; Kim, Kun Suk ; Yoo, Han-Wook

Hormone research in paediatrics, 2010, Vol.73 (1), p.41-48 [Periódico revisado por pares]

Switzerland

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