Results 131 to 140 of about 1,914,079 (156)

Tubulointerstitial nephritis and uveitis syndrome in a patient with diabetic nephropathy: a case report and literature review. [PDF]

Front Med (Lausanne)
Deng DF, Lin LM, Wang L, Wang CJ, Wei ZP, Wu YP, Wang XQ, Zou XR.   +7 more
europepmc   +1 more source

Automated bone age assessment in rare pediatric growth disorders: a comparative study using Deeplasia. [PDF]

Front Endocrinol (Lausanne)
Skaf K, Fardipour M, Schmidt P, Bolmer E, Keller A, Lampe C, Jurgens J, Lindschau M, Palm K, Ruckdeschel S, Javanmardi B, Mohnike K.   +11 more
europepmc   +1 more source

Growth Hormone Therapy in Children Born Small for Gestational Age with Persistent Short Stature: Lessons Learned from Real-World International Databases and Directions for Future Research.

Horm Res Paediatr
Samvelyan S, Ahmed SF, Alimussina M, Kodytkova A, Jirova B, Amaratunga SA, Lebl J.   +6 more
europepmc   +1 more source

Imprinting Disorders and Epigenetic Alterations in Children Conceived by Assisted Reproductive Technologies: Mechanisms, Clinical Outcomes, and Prenatal Diagnosis. [PDF]

Genes (Basel)
Gambadauro A, Chirico V, Galletta F, Gulino F, Chimenz R, Serraino G, Rulli I, Manganaro A, Gitto E, Marseglia L.   +9 more
europepmc   +1 more source

Silver-Russell syndrome and exclusion of uniparental disomy

Clinical Genetics, 1996
Recently maternal uniparental disomy for the entire chromosome 7 was described in three of 25 Silver-Russell syndrome sporadic cases, yet the etiology of the remaining cases is unclear.
L G Shaffer
exaly   +2 more sources

Silver-Russell syndrome as a cause for early intrauterine growth restriction

Prenatal Diagnosis, 2005
The diagnosis of Silver-Russell syndrome is based on the characteristic growth restriction and the presence of typical dysmorphic features. We present the prenatal and postnatal findings of a case that was treated at our perinatal center.
Birgit Seelbach-Göbel
exaly   +2 more sources

Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell–Silver syndrome

American Journal of Medical Genetics, Part A, 2016
Russell-Silver syndrome is a heterogeneous disorder characterized by intrauterine growth retardation, postnatal growth deficiency, characteristic facial appearance, and other variable features.
Dimitri Stavropoulos, Cheryl Cytrynbaum, Stephen W Scherer   +2 more
exaly   +2 more sources

Some of the next articles are maybe not open access.

Related searches:

Intellectual functioning in Silver-Russell syndrome: First study in adults

Applied Neuropsychology Adult, 2021
Genavee Brown, Irene NETCHINE, Mélissa Burgevin   +2 more
exaly