Results 121 to 130 of about 1,914,079 (156)

Colorectal cancer in a man with silver-Russell syndrome: a case report. [PDF]

Oxf Med Case Reports
Ibraik F, Hammouri I, Arafat H, Hammouri AG, Qahoush H.   +4 more
europepmc   +1 more source

Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype Correlation. [PDF]

Clin Genet
Licata AM, Botzenhart E, Kloth-Stachnau K, Eggermann T.   +3 more
europepmc   +1 more source

A rapid review of genetic association studies of parent-of-origin effects and fetal growth. [PDF]

Mol Cell Pediatr
Kang EJW, Dewan AT.
europepmc   +1 more source

Multilesional pyoderma gangrenosum secondary to Hodgkin lymphoma. [PDF]

JAAD Case Rep
McDaniel K, Karunakaran S, Upton L, Russell L, Heinecke G, Burkemper N.   +5 more
europepmc   +1 more source

SARS-CoV-2 seroprevalence among pregnant women during the first three waves of the COVID-19 pandemic in southern Mozambique. [PDF]

BMC Pregnancy Childbirth
Sevene E, Maculuve S, Tchavana C, Valá A, Quimice L, Macuacua S, Carrilho C, Gonzalez R, Nhampossa T, Menendez C, Craik R, Hookham L, Le Doare K, von Dadelszen P, periCOVID-Africa and PRECISE Network.   +14 more
europepmc   +1 more source

Hypomethylation of the MEG8:Int2-DMR  in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome [PDF]

Clin Epigenetics
D'Angelo E, Pignata L, Cecere F, Vimercati A, Cubellis MV, Saadat A, Giaccari C, Thibaud N, Eggermann T, Fernández JR, Russo S, Netchine I, Cerrato F, Riccio A, Brioude F.   +14 more
europepmc   +2 more sources

Eosinophilic, polymorphic, and pruritic eruption associated with radiation treated with dupilumab in a patient with Hodgkin lymphoma. [PDF]

JAAD Case Rep
Hartman M, Russell L, Goyal S, Burkemper N, Heinecke G, Hurley MY, Smith K, Smith EH.   +7 more
europepmc   +1 more source

Short-term Safety Profile of Trochanteric-Entry Intramedullary Lengthening Nails in Skeletally Immature Patients. [PDF]

J Pediatr Soc North Am
Bram JT, Troyer S, Murphy EP, Fragomen AT, Reif T, Hoellwarth JS, Rozbruch SR.   +6 more
europepmc   +1 more source

21-Hydroxylase Deficient Congenital Adrenal Hyperplasia Due to Maternal Uniparental Isodisomy. [PDF]

Case Rep Endocrinol
Kluge ML, Schema L, Schroepfer K, Thoreson EK, Sarafoglou K, Rowsey RA, Marcou CA, Moyer AM, Schultz MJ.   +8 more
europepmc   +1 more source

Clinical and genetic diagnosis and management of Silver-Russell syndrome: Report of four cases. [PDF]

World J Clin Pediatr
Toulia I, Savvidou P, Ververi A, Grammatikopoulou MG, Kosta K, Tziaferi V, Antachopoulos C, Goulis DG, Sotiriadis A, Tsiroukidou K.   +9 more
europepmc   +1 more source