An unusual brain lesion in a patient with Laron Syndrome
L Kornreich, Z Laron - Endocrine, 2024 - Springer
Dear Editor, Referring to the article by Zhou et al.[1] reporting brain white matter alterations
in adult patients with childhoodonset Growth Hormone (GH) deficiency, we herewith report …
in adult patients with childhoodonset Growth Hormone (GH) deficiency, we herewith report …
Laron syndrome in three female siblings with the development of subclinical hypothyroidism and dyslipidemia in one case: first report of a Syrian family
A Chreitah, K Hijazia, LJ Doya - Oxford Medical Case Reports, 2021 - academic.oup.com
Laron syndrome (LS) is a rare autosomal recessive disorder characterized by dwarfism and
typical facial phenotype. This report is the first to present three cases of Laron syndrome …
typical facial phenotype. This report is the first to present three cases of Laron syndrome …
Effect of Ethanol Consumption on the Placenta and Liver of Partially IGF-1-Deficient Mice: The Role of Metabolism via CYP2E1 and the Antioxidant Enzyme System
I Martín-Estal, ÓR Fajardo-Ramírez… - Biology, 2022 - mdpi.com
Simple Summary Ethanol is the most consumed drug worldwide, even during pregnancy.
One of its adverse outcomes is fetal growth restriction, an alteration in development due to …
One of its adverse outcomes is fetal growth restriction, an alteration in development due to …
Long-term treatment with recombinant human growth hormone in pediatric patients with growth hormone deficiency influences but does not destroy stem cells …
A Wedrychowicz, K Sielatycka, M Kucia, E Kubis… - 2024 - researchsquare.com
Long-term treatment with recombinant human growth hormone in pediatric patients with growth
hormone deficiency influences but do Page 1 Page 1/15 Long-term treatment with recombinant …
hormone deficiency influences but do Page 1 Page 1/15 Long-term treatment with recombinant …
[HTML][HTML] Diagnosis of Laron syndrome using monoplex-polymerase chain reaction technology with a whole-genome amplification template: A case report
A Neumann, MÁ Alcántara-Ortigoza… - World Journal of …, 2019 - ncbi.nlm.nih.gov
BACKGROUND Laron syndrome (LS) is an autosomal recessive hereditary condition
affecting only 1/1000000 births. The cause is associated with mutations in the growth …
affecting only 1/1000000 births. The cause is associated with mutations in the growth …
Síndrome de larón e inmunidad al cáncer y la diabetes
SC Pin, NV Cedeño, D Callejas - Revista Científica Arbitrada …, 2022 - editorialalema.org
El Síndrome de Laron o Enanismo tipo Laron, también llamado Insensibilidad a la Hormona
del Crecimiento (IGH), es una enfermedad rara, congénita, autosómica recesiva que no …
del Crecimiento (IGH), es una enfermedad rara, congénita, autosómica recesiva que no …
[PDF][PDF] SÍNDROME DE LARÓN E INMUNIDAD AL CÁNCER Y LA DIABETES LARON SYNDROME AND IMMUNITY TO CANCER AND DIABETES
SC Pin, NV Cedeño, D Callejas - researchgate.net
El Síndrome de Laron o Enanismo tipo Laron, también llamado Insensibilidad a la Hormona
del Crecimiento (IGH), es una enfermedad rara, congénita, autosómica recesiva que no …
del Crecimiento (IGH), es una enfermedad rara, congénita, autosómica recesiva que no …
[PDF][PDF] A case of short stature found to be Laron Syndrome: A case report.
YO Kabli, AE Al-Agha, MA Shazly - researchgate.net
Laron Syndrome (LS) is an autosomal recessive disorder that causes short stature due to
growth hormone insensitivity, despite the high levels of growth hormone [1-3]. Since its first …
growth hormone insensitivity, despite the high levels of growth hormone [1-3]. Since its first …