| Ident. | Authors (with country if any) | Title |
|---|
| 000567 |
Aisling M. O'Riordan [Irlande (pays)] ; Niamh Mcgrath [Irlande (pays)] ; Farhana Sharif [Irlande (pays)] ; Nuala P. Murphy [Irlande (pays)] ; Orla Franklin [Irlande (pays)] ; Sally Ann Lynch [Irlande (pays)] ; Michael J. O'Grady [Irlande (pays)] | Expanding the clinical spectrum of chromosome 15q26 terminal deletions associated with IGF-1 resistance. |
| 000C17 |
Rita Espírito Santo [Portugal] ; Oana Moldovan [Portugal] ; Paula Costa [Portugal] ; André Graça [Portugal] ; Margarida Abrantes [Portugal] | Puffy feet in a female neonate. |
| 001501 |
Fatma Bastaki [Émirats arabes unis] ; Madiha Mohamed [Émirats arabes unis] ; Pratibha Nair [Émirats arabes unis] ; Fatima Saif [Émirats arabes unis] ; Nafisa Tawfiq [Émirats arabes unis] ; Mahmoud Taleb Al-Ali [Émirats arabes unis] ; Oliver Brandau [Allemagne] ; Abdul Rezzak Hamzeh [Émirats arabes unis] | A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis-lymphedema-telangiectasia syndrome by Whole Exome Sequencing. |
| 001A41 |
Elisavet Fotiou [Royaume-Uni] ; Silvia Martin-Almedina [Royaume-Uni] ; Michael A. Simpson [Royaume-Uni] ; Shin Lin [États-Unis] ; Kristiana Gordon [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Giles Atton [Royaume-Uni] ; Iona Jeffery [Royaume-Uni] ; David C. Rees [Royaume-Uni] ; Cyril Mignot [France] ; Julie Vogt [Royaume-Uni] ; Tessa Homfray [Royaume-Uni] ; Michael P. Snyder [États-Unis] ; Stanley G. Rockson [États-Unis] ; Steve Jeffery [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Pia Ostergaard [Royaume-Uni] | Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis |
| 002164 |
Cyprien Zaré [Burkina Faso] ; Ibrahim Alain Traoré [Burkina Faso] ; Patrick Wendpuoiré Hamed Dakouré [Burkina Faso] ; Salif Gandéma [Burkina Faso] ; Bakary Gustave Sano [Burkina Faso] ; Lazard Bouma Bénao [Burkina Faso] ; Hermann Belemlilga [Burkina Faso] ; Nassirou Yabré [Burkina Faso] | Amniotic band syndrom at Bobo Dioulasso university teaching hospital (Burkina-Faso): about two cases |
| 002872 |
Pierre Navarre [Canada] ; Benoit Poitras | Lymphoedema in tuberous sclerosis: case report and review of the literature. |
| 002878 |
Reid A. Maclellan [États-Unis] ; Arin K. Greene [États-Unis] | Lymphedema. |
| 004000 |
Kaz M Gezginç ; Fatma Yaz C ; Dilay Gök | Prenatal diagnosis of Milroy's primary congenital lymphedema. |
| 004070 |
Siham Al Sinani ; Yusria Al Rawahi ; Hamed Abdoon | Octreotide in Hennekam syndrome-associated intestinal lymphangiectasia |
| 004122 |
Natalia Pastora [Espagne] ; Jesus Peralta ; Irene Canal-Fontcuberta ; Anna Grabowska ; Jose S. Pulido ; Jose Abelairas ; Felix Armada ; Alfredo Garcia-Alix | Microcephaly-lymphedema-chorioretinal dysplasia associated with pachymicrogyria and atrophy of the cerebellar vermis: an integration of brain-ocular migration disorders. |
| 004257 |
Gwendolyn De Bruyn [Belgique] ; Alexandra Casaer ; Katrien Devolder ; Geert Van Acker ; Hilde Logghe ; Koen Devriendt ; Luc Cornette | Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression. |
| 004416 |
C. Bellini [Italie] ; Z. Ergaz ; M. Radicioni ; I. Forner-Cordero ; M. Witte ; G. Perotti ; T. Figar ; L. Tubaldi ; P. Camerini ; B. Bar-Oz ; I. Yatsiv ; I. Arad ; F. Traverso ; T. Bellini ; F. Boccardo ; C. Campisi ; P. Dalmonte ; N. Vercellino ; S. Manikanti ; E. Bonioli | Congenital fetal and neonatal visceral chylous effusions: neonatal chylothorax and chylous ascites revisited. A multicenter retrospective study. |
| 004418 |
Subham Bhattacharya ; Niloy Kr Das ; Anirban Chatterjee | Congenital chylous ascites and lymphedema in Down's syndrome. |
| 004935 |
Jan Kazenwadel [Australie] ; Genevieve A. Secker [Australie] ; Yajuan J. Liu [États-Unis] ; Jill A. Rosenfeld [États-Unis] ; Robert S. Wildin [États-Unis] ; Jennifer Cuellar-Rodriguez [États-Unis] ; Amy P. Hsu [États-Unis] ; Sarah Dyack [États-Unis] ; Conrad V. Fernandez [États-Unis] ; Chan-Eng Chong [Australie] ; Milena Babic [Australie] ; Peter G. Bardy [Australie] ; Akiko Shimamura [États-Unis] ; Michael Y. Zhang [États-Unis] ; Tom Walsh [États-Unis] ; Steven M. Holland [États-Unis] ; Dennis D. Hickstein [Australie] ; Marshall S. Horwitz [États-Unis] ; Christopher N. Hahn [Australie] ; Hamish S. Scott [Australie] ; Natasha L. Harvey [Australie] | Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature |
| 004966 |
A. Maruani [France] ; M. Samimi ; G. Lorette | [Port-wine stains of the limbs]. |
| 004C97 |
Pia Ostergaard [Royaume-Uni] ; Michael A. Simpson ; Fiona C. Connell ; Colin G. Steward ; Glen Brice ; Wesley J. Woollard ; Dimitra Dafou ; Tatjana Kilo ; Sarah Smithson ; Peter Lunt ; Victoria A. Murday ; Shirley Hodgson ; Russell Keenan ; Daniela T. Pilz ; Ines Martinez-Corral ; Taija Makinen ; Peter S. Mortimer ; Steve Jeffery ; Richard C. Trembath ; Sahar Mansour | Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). |
| 005247 |
John S. Ferguson [Royaume-Uni] ; Shymalar Gunatheesan [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Rob Hastings [Royaume-Uni] ; Ruth Newbury-Ecob [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] | Primary lymphedema with coarctation of the aorta: Possible new syndrome or variant of Irons–Bianchi syndrome? |
| 005249 |
J. Benard [France] ; J. Saada [France] ; J. Amiel [France] ; S. Vignes [France] ; A. Benachi [France] ; O. Picone [France] | Prenatal diagnosis of Milroy disease |
| 005346 |
María Perez-Crespo [Espagne] ; Isabel Betlloch [Espagne] ; Maria Teresa Martinez-Miravete [Espagne] ; Irene Ballester [Espagne] ; Ana Lucas [Espagne] ; Javier Mataix [Espagne] | Congenital Lower Limb Enlargement in a Newborn |
| 005499 |
Isabelle Quéré [France] | [Lymphatic system: Anatomy, histology and physiology]. |
| 005514 |
Nicole A J. De La Haye [Pays-Bas] ; Monique M. Den Ouden | [A newborn with swollen feet]. |
| 005682 |
M. Todd [Royaume-Uni] ; J. Welsh ; M W Drummond | Primary lymphedema and acute leukemia--is there a link? |
| 005970 |
Yoshinori Ozeki ; Yoshiaki Shimada ; Atsuhiro Tanikawa ; Masayuki Horiguchi ; Masatomo Takeuchi ; Toshio Yamazaki | Congenital toxoplasmosis mimicking microcephaly-lymphedema-chorioretinal dysplasia. |
| 005F28 |
Bei-Yan Zhou ; Guang-Jin Lu ; Yu-Kun Han | [Congenital lower limb lymphedema in a neonate]. |
| 006005 |
P J Hooper [États-Unis] ; M H Bradley ; G. Biswas ; E A Ottesen | The Global Programme to Eliminate Lymphatic Filariasis: health impact during its first 8 years (2000-2007). |
| 006599 |
Smadar Eventov-Friedman [Israël] ; Amihood Singer [Israël] ; Eric S. Shinwell [Israël] | Microcephaly, lymphedema, chorioretinopathy and atrial septal defect: a case report and review of the literature |
| 006D71 |
Glen Brice [Royaume-Uni] | Perinatal diagnosis of a lymphoedema‐distichiasis syndrome |
| 006D72 |
Corradino Campisi [Italie] ; Elisa Da Rin [Italie] ; Carlo Bellini [Italie] ; Eugenio Bonioli [Italie] ; Francesco Boccardo [Italie] | Pediatric lymphedema and correlated syndromes: Role of microsurgery |
| 007488 |
M. Büchner [Allemagne] ; S. Dostert [Allemagne] ; A. Falkert [Allemagne] ; G. Huber [Allemagne] ; B. Seelbach-Göbel [Allemagne] | Perinatal diagnosis of a lymphedema‐distichiasis syndrome (LD) |
| 007819 |
Salem Samra [États-Unis] ; Asaad H. Samra ; David T. Netscher | Threatened lower extremity in a neonate from a severely constricting amniotic band: a case for limb salvage after a 6-year functional follow-up. |
| 007B94 |
Natalia Pastor [Espagne] ; Isabel Betlloch [Espagne] ; Mar Blanes [Espagne] ; Javier Mataix [Espagne] ; José Ba Uls [Espagne] ; Isabel Belinch N [Espagne] | Noonan Syndrome and Scrotal Lymphedema: Primary or Secondary? |
| 007C66 |
David A. Stevenson [États-Unis] ; Theodore J. Pysher [États-Unis] ; Robert M. Ward [États-Unis] ; John C. Carey [États-Unis] | Familial congenital non‐immune hydrops, chylothorax, and pulmonary lymphangiectasia |
| 007E91 |
A. Debeer [Belgique] ; E. Steenkiste ; K. Devriendt ; M. Morren | Scalp skin lesion in Turner syndrome: more than lymphoedema? |
| 007F44 |
Pradeep C. Vasudevan [Royaume-Uni] ; Sixto Garcia-Minaur ; Maria Pilar Botella ; Antonio Perez-Aytes ; Nora L. Shannon ; Oliver W J. Quarrell | Microcephaly-lymphoedema-chorioretinal dysplasia: three cases to delineate the facial phenotype and review of the literature. |
| 008357 |
Etty Daniel-Spiegel [Israël] ; Arash Ghalamkarpour [Belgique] ; Ronen Spiegel [Israël] ; Ehud Weiner [Israël] ; Miikka Vikkula [Belgique] ; Eliezer Shalev [Israël] ; Stavit Alon Shalev [Israël] | Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema |
| 008790 |
Jeffrey S. Upperman [États-Unis] ; Edward M. Barksdale | Images in clinical medicine. Congenital lymphedema. |
| 008793 |
J-C Tille [Suisse] ; M S Pepper | Hereditary vascular anomalies: new insights into their pathogenesis. |
| 008796 |
C. Campisi [Italie] ; S. Michelini ; F. Boccardo | Guidelines of the Societá Italiana di Linfangiologia: excerpted sections. |
| 008D62 |
Cheickna Sylla [Sénégal] ; Babacar Diao ; Abdoulaye Bobo Diallo ; Papa Ahmed Fall ; Anne Aurore Sankale ; Mamadou Ba | [Complications of circumcision. Report of 63 cases]. |
| 008F13 |
Astrid Imiela [France] ; Delphine Salle-Staumont ; Georges-Marie Breviere ; Benoit Catteau ; Veronique Martinot-Duquennoy ; Frederic Piette | Congenital elephantiasis-like lymphangiomatosis of a lower limb. |
| 009268 |
Martin Frühwirth [Autriche, États-Unis, Royaume-Uni, Norvège] ; Andreas R. Janecke ; Thomas Müller ; Victoria E. H. Carlton ; Florian Kronenberg ; Felix Offner ; A. S. Knisely ; Silvana Geleff ; Eyun J. Song ; Burkhard Simma ; Alfred Königsrainer ; Raimund Margreiter ; C. B. Van Der Hagen ; Kristin Eiklid ; Ystein Aagenaes ; Laura Bull ; Helmut Ellemunter | Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome |
| 009886 |
Carlo Bellini [Italie] ; Cesare Arioni [Italie] ; Massimo Mazzella [Italie] ; Corradino Campisi [Italie] ; Gioconda Taddei [Italie] ; Francesco Boccardo [Italie] ; Giovanni Serra [Italie] | Lymphoscintigraphic evaluation of congenital lymphedema of the newborn |
| 009941 |
A. Heiberg | [Aagenaes syndrome--lymphedema and intrahepatic cholestasis]. |
| 009E93 |
S. Mansour [Royaume-Uni] ; H. Woffendin [Royaume-Uni] ; S. Mitton [Royaume-Uni] ; I. Jeffery [Royaume-Uni] ; T. Jakins [Royaume-Uni] ; S. Kenwrick [Royaume-Uni] ; V. A. Murday [Royaume-Uni] | Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection |
| 00A043 |
I. Casteels [Belgique] ; K. Devriendt [Belgique] ; I. Casteels [Belgique] ; K. Devriendt [Belgique] ; A. Leys [Belgique] ; H. Van Cleynenbreugel [Belgique] ; P. Demaerel [Belgique] ; F. De Tavernier [Belgique] ; J P Fryns [Belgique] ; P. Demaerel [Belgique] ; F. De Tavernier [Belgique] ; J P Fryns [Belgique] | Autosomal dominant microcephaly—lymphoedema-chorioretinal dysplasia syndrome |
| 00A112 |
David N. Finegold [États-Unis] ; Mark A. Kimak [États-Unis] ; Elizabeth C. Lawrence [États-Unis] ; Kara L. Levinson [États-Unis] ; Elizabeth M. Cherniske [États-Unis] ; Barbara R. Pober [États-Unis] ; Jean W. Dunlap [États-Unis] ; Robert E. Ferrell [États-Unis] | Truncating mutations in FOXC2 cause multiple lymphedema syndromes |
| 00A175 |
P. Huppke [Allemagne] ; H J Christen ; B. Sattler ; F. Hanefeld | Two brothers with Hennekam syndrome and cerebral abnormalities. |
| 00A269 |
H. Nogami [Japon] ; H. Ito ; K. Arao ; T. Oki ; M. Futamura | Congenital balloon digits in two neonates caused by constriction rings. |
| 00B006 |
C. M. Papendieck [Argentine] | Hair Tourniquet syndrome : An unusual cause of perinatologic secondary lymphedema |
| 00B047 |
J P Fryns ; P. Moerman | Trisomy 21 in a second trimester male hydropic fetus with "Noonan-syndrome-phenotype": nuchal and thoracic lymphangiomatosis, oedema of the dorsum of hands and feet, and bicuspid pulmonary valve. |
| 00B120 |
P R Nj Lstad [Norvège] ; H. Reigstad ; J. Westby ; A. Espeland | Familial non-immune hydrops fetalis and congenital pulmonary lymphangiectasia. |
| 00B687 |
R. J. Bolt [Pays-Bas] ; W. Peelen [Pays-Bas] ; P. G. J. Nikkels [Pays-Bas] ; T. P. V. M. De Jong [Pays-Bas] | Congenital lymphoedema of the genitalia |
| 00BB02 |
Brad Angle [États-Unis] ; Joseph H. Hersh [États-Unis] | Expansion of the phenotype in Hennekam syndrome: A case with new manifestations |
| 00BC67 |
C. Kozma [États-Unis] ; N. Scribanu ; E. Gersh | The microcephaly-lymphoedema syndrome: report of an additional family. |
| 00BF48 |
Elizabeth K. Schorry [États-Unis] ; Anne M. Lovell [États-Unis] ; Athena Milatovich [États-Unis] ; Howard M. Saal [États-Unis] | Ullrich‐Turner syndrome and neurofibromatosis‐1 |
| 00BF55 |
K. Mishima [Japon] ; T. Sugahara [Japon] ; Y. Mori [Japon] ; M. Sakuda [Japon] | Three cases of oblique facial cleft |
| 00C091 |
Emily Chen ; Susan K. Larabell ; Jamilyn M. Daniels [États-Unis] ; Stanley Goldstein [États-Unis] | Distichiasis‐lymphedema syndrome: Tetralogy of Fallot, chylothorax, and neonatal death |
| 00C237 |
C. Sohn ; C. J Hnichen ; G. Bastert | [Effectiveness of beta-hydroxyethylrutoside in patients with varicose veins in pregnancy]. |
| 00C310 |
N. Weinzweig [États-Unis] | Constriction band-induced vascular compromise of the foot: classification and management of the "intermediate" stage of constriction-ring syndrome. |
| 00C327 |
R P Erickson [États-Unis] ; L. Hudgins ; J F Stone ; S. Schmidt ; C. Wilke ; T W Glover | A "balanced" Y;16 translocation associated with Turner-like neonatal lymphedema suggests the location of a potential anti-Turner gene on the Y chromosome. |
| 00C535 |
A. Villa [Espagne] ; M. Urioste ; M. C. Carrascosa [Espagne] ; S. Vázquez [Espagne] ; A. Martínez [Espagne] ; M. L. Martínez-Frías [Espagne] | Pericentric inversions of chromosome 4: report of a new family and review of the literature |
| 00C820 |
H. Güvenc [Turquie] ; A D Aygün ; K. Kocabay ; D. Türkbay ; W W Tunnessen | Picture of the month. Turner's syndrome. |
| 00CC01 |
M L Eberhard [États-Unis] ; W L Hitch ; D F Mcneeley ; P J Lammie | Transplacental transmission of Wuchereria bancrofti in Haitian women. |
| 00CC24 |
V L Katz ; B. Kort ; W J Watson | Progression of nonimmune hydrops in a fetus with Noonan syndrome. |
| 00CC92 |
T R Campello [Brésil] ; R S Ferreira ; M L Pires ; P G De Melo ; R. Albuquerque ; S. Araujo ; G. Dreyer | A study of placentas from Wuchereria bancrofti microfilaraemic and amicrofilaraemic mothers. |
| 00CC95 |
S R Phaoke [Inde] ; A K Sharma ; S S Agarawal | A new syndrome of multiple joint dislocations with metaphyseal dysplasia. |
| 00CE47 |
G. Nigro [Italie] ; A. Clerico [Italie] ; C. Mondaini [Italie] | Symptomatic congenital cytomegalovirus infection in two consecutive sisters. |
| 00D046 |
M. Jernite [France] ; L. Donato ; R. Favre ; J. Haddad ; M. Esposito ; J. Messer | [Medical treatment of chylous effusions in newborn infants. Apropos of 3 cases]. |
| 00D436 |
P. Govaert [Belgique] ; J. G. Leroy ; R. Pauwels ; P. Vanhaesebrouck ; C. De Praeter ; H. Van Kets ; M. Goeteyn | Perinatal manifestations of maternal yellow nail syndrome |
| 00D515 |
D. Lacombe [France] ; A. Taieb ; P. Masson ; M. Fayon ; J L Demarquez | Neonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp. |
| 00D719 |
C. D. M. Fletcher [Royaume-Uni] ; A. Beham [Royaume-Uni, Autriche] ; C. Schmid [Royaume-Uni, Autriche] | Spindle cell haemangioendothelioma: a clinicopathological and immunohistochemical study indicative of a non‐neoplastic lesion |
| 00D820 |
Miguel Urioste [Espagne] ; Antonio Arroyo [Espagne] ; María-Luisa Martínez-Frías [Espagne] | Campomelia, polycystic dysplasia, and cervical lymphocele in two sibs |
| 00D882 |
G. Har-El [États-Unis] ; M. L. Borderon ; M. H. Weiss | Choanal atresia and lymphedema |
| 00D909 |
L. Hanssler ; K A Metz ; C. Roll ; K H Hennecke | [Primary lymphatic dysplasia in a newborn infant]. |
| 00D988 |
M J Edwards ; J M Graham | Posterior nuchal cystic hygroma. |
| 00DB76 |
G. I. Muguti [Zimbabwe] | The amniotic band syndrome: single-stage correction |
| 00DD78 |
W J Scheijgrond [Pays-Bas] ; R. Rodrigues Pereira ; R J Roorda ; F H Jansen | [Early amnion rupture as a cause of multiple congenital abnormalities in the newborn infant]. |
| 00DD89 |
A. La Capria ; C. Mongioy ; F. Balossini ; M. Zilioli ; P U Falzoni ; F. Giorgini ; G. Sorrentino | [Amniotic band syndrome. Clinico-therapeutic considerations on 3 cases]. |
| 00E001 |
Clive Levine [États-Unis] | Primary disorders of the lymphatic vessels—A unified concept |
| 00E192 |
P. Sarda [France] ; J. Jalaguier ; F. Montoya ; H. Bonnet | [Hereditary congenital lymphedema with pseudosexual ambiguity]. |
| 00E236 |
H M Saal [États-Unis] ; K N Rosenbaum | Screening the newborn for anatomic and metabolic defects. |
| 00E605 |
B R Benacerraf ; F D Frigoletto | Prenatal sonographic diagnosis of isolated congenital cystic hygroma, unassociated with lymphedema or other morphologic abnormality. |
| 00E805 |
David R. Witt [États-Unis] ; H. Eugene Hoyme [États-Unis] ; Jonathan Zonana [États-Unis] ; David K. Manchester [États-Unis] ; Jean Pierre Fryns [Belgique] ; J. Geoffrey Stevenson [États-Unis] ; Cynthia J. R. Curry [États-Unis] ; Cynthia J. R. Hall ; John M. Opitz ; James F. Reynolds | Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature |
| 00E843 |
J. Rosenthal [Israël] ; D. Abeliovich [Israël] ; D. Carmi [Israël] ; John M. Opitz ; James F. Reynolds | Clinical variability of partial duplication 1q: A clinical report and literature review |
| 00E854 |
P. Chen [États-Unis] ; Enrique Gonzalez [États-Unis] ; John M. Opitz ; James F. Reynolds | Amniotic band sequence and its neurocutaneous manifestations |
| 00E920 |
H J Voigt ; U. Claussen ; R. Ulmer | [Fetal neck edema--early sonographic indications of a chromosome abnormality]. |
| 00E971 |
C G Magnusson ; J Y Cesbron ; R. Djurup ; A. Capron ; S G Johansson | Raised serum IgG4 levels in patients with atopy and filariasis: application of an automated particle-counting immunoassay using monoclonal antibody. |
| 00E997 |
M H Witte ; C L Witte | Lymphangiogenesis and lymphologic syndromes. |
| 00EC09 |
Carol A. Crowe [États-Unis] ; Lois H. Dickerman [États-Unis] ; John M. Opitz [États-Unis] ; James F. Reynolds [États-Unis] | Brief clinical report: A genetic association between microcephaly and lymphedema |
| 00F060 |
P H Schober ; M. Kratky ; W D Müller | [You make the diagnosis: congenital hereditary lymphedema]. |
| 00F122 |
G J Merli | Lymphedema. |
| 00F139 |
E A Andersen ; J. Hertel ; S A Pedersen ; H R S Rensen | Congenital chylothorax: management by ligature of the thoracic duct. |
| 00F593 |
M. Gatniejewska-Komraus ; A. Bo Kowski | [Hyperbilirubinemia in congenital lymphedema]. |
| 00F621 |
A A Adeyokunnu | The incidence of Turner's syndrome in Ibadan, Nigeria. |
| 00F721 |
Anthony Shaw [États-Unis] ; Kuldeep Teja [États-Unis] | Two infants with an unusual constellation of angiomatous anomalies |
| 00F774 |
Frank M. Guttman [Canada] ; Phillipe Montupet [Canada] ; Robert S. Bloss [Canada] | Experience with peritoneo-venous shunting for congenital chylous ascites in infants and children |
| 00FA57 |
H M Henriksen | Turners's syndrome associated with lymphoedema, diagnosed in the newborns. |
| 00FD15 |
| Anasarca in the newborn. |
| 00FE46 |
P L Roberi ; P. Bini ; L. Zannino ; E. Rossi | [Hereditary lymphedema (Milroy's disease). Case contribution]. |
| 010056 |
G. Vadász ; V. Groák | [A case of Milroy's disease]. |
| 010567 |
J. Delacrétaz ; E. Frenk ; A. Christeler ; B. Tapernoux | [Demonstrations]. |
| 010904 |
W. Lukas ; K. Jo Czyk ; A. Sychlowy ; D. Pawelek-Krombholz | [Congenital generalized lymphedema]. |
| 010A27 |
H E Köhnlein | [Significance of plastic surgery today]. |
| 010A83 |
C J Baker ; A J Rudolph | Congenital ring constrictions and intrauterine amputations. |
| 010B68 |
P. Peller ; J. Schaub ; H. Zobel ; H J Bremer | [Intestinal lymphangiectasis]. |
| 010F71 |
D H Carr ; R A Haggar ; A G Hart | Germ cells in the ovaries of XO female infants. |
| 011093 |
F. Schmidt | [Labor complications due to fetal megacystis]. |
| 011100 |
K. Bartkowiak ; J. Mikolajczyk | [Edemas of Nonne-Milroy]. |
| 011295 |
B K Rank ; G S Wong | Lipoedema. |
| 011325 |
Malcolm H. Gough [Royaume-Uni] | Primary lymphoedema: Clinical and lymphangiography studies |
| 011E26 |
O. Orsini ; O G Costa | [Secondary elephantiasis caused by streptococci in congenital annular constriction bands]. |
| 012393 |
M L Pires [Brésil] ; R S Ferreira ; S. Araújo ; R. Albuquerque ; J. Remigio Neto ; A S Da Silva ; G. Dreyer | [Transplacental passage of Wuchereria bancrofti microfilariae in newborns of microfilaremic mothers]. |
| 012413 |
B. Salazard [France] ; J. Londner ; D. Casanova ; J. Bardot ; G. Magalon | [The lymphatic malformations: clinical aspects and evolution]. |
| 012542 |
Guido La Placa [Italie] ; Massimo Andreotti ; Claudio Pradella ; Fiorella Russo ; Roberto Besana | [Nonne-Milroy's syndrome (hereditary lymphedema type I). Report of a clinical case]. |
| 012666 |
C H Gonzalez ; H B Corradini ; P H Saladanha | [Identification of Turner's syndrome in the newborn infant]. |
| 012675 |
R. Lisker ; F. De María Herrera ; J. Ocaranza | [Hereditary congenital lymphedema]. |
| 012761 |
J D Picard ; C. Polonovski ; J P Gallet ; R. Laplane | [Congenital lymphedema]. |
| 012837 |
C. Beluschi ; M. Coraiola ; D. Pedrotti | [A case of congenital hereditary lymphedema (Milroy-Nonne's disease]. |
| 012A06 |
C. Severien ; S. Felix ; K. Bartholomé | Ring chromosome 22: a case report. |
| 012A60 |
Siba Prosad Paul ; Michael A. Patton | Presentation one: a neonate with swollen feet. |
| 012A93 |
Daniela Larizza [Italie] ; Miryam Martinetti ; Jean Michel Dugoujon ; Carmine Tinelli ; Valeria Calcaterra ; Mariaclara Cuccia ; Laura Salvaneschi ; Francesca Severi | Parental GM and HLA genotypes and reduced birth weight in patients with Turner's syndrome. |
| 012C96 |
Valerie M. Carlberg [États-Unis] ; Sabra M. Lofgren ; Julianne A. Mann ; Jared P. Austin ; Dawn Nolt ; Evan B. Shereck ; Blachy Davila-Saldana ; Jonathan Zonana ; Alfons L. Krol | Hypohidrotic ectodermal dysplasia, osteopetrosis, lymphedema, and immunodeficiency in an infant with multiple opportunistic infections. |
| 012E20 |
N. Krywonis ; V N Kaye ; P J Lynch | Cryptococcal cellulitis in congenital lymphedema. |
| 012E39 |
P. Chaturvedi ; B. Advani ; A A Khan ; B C Harinath ; A. Gawdi | Congenital filarial lymphoedema. |
| 012E90 |
O H Haugen [Norvège] ; J. Krohn | Bilateral congenital glaucoma in a child with hydrops fetalis, congenital pulmonary lymphangiectasia, and lymphoedema. |
| 012F17 |
E. Boudon [France] ; Y. Levy [France] ; T. Abossolo [France] ; François Cartault [France] ; P. Brouillard [Belgique] ; M. Vikkula [Belgique] ; M. Kieffer-Traversier [France] ; D. Ramful [France] ; J L Alessandri [France] | Antenatal presentation of hereditary lymphedema type I. |
